Johnson & Johnson
JNJHealthcare|Drug Manufacturers - General|USA
$240.97
-2.07 (-0.85%)
DCF (FCF)
$109.52
Earnings Power
$76.17
Clinical Trials (500)
| Trial | Conditions | Phase | Status | Enrollment | Design | Drug |
|---|---|---|---|---|---|---|
| NCT07225101 Evaluation of the Efficacy of STRATAFIX for Neurosurgical Cranial and Spine Procedures | Wound Closure, Brain Tumor Adult | P4 | Recruiting | 160 | Open-label | — |
| NCT03229200 Extended Treatment Protocol for Subjects Continuing to Benefit From Ibrutinib. | Lymphoma, B-Cell, Lymphoma, Non-Hodgkin | P4 | Active | 297 | Open-label | Ibrutinib |
| NCT07141004 A Study of Guselkumab Administered Subcutaneously in Treatment of Indian Participants With Psoriatic Arthritis (PsA) | Arthritis, Psoriatic | P4 | Recruiting | 100 | Open-label | Guselkumab |
| NCT04892173 JNJ-90301900 (NBTXR3) Activated by Radiotherapy With or Without Cetuximab in LA-HNSCC | Locally Advanced Head and Neck Squamous Cell Carcinoma, Aged | P3 | Recruiting | 500 | RCT, Open-label | JNJ-90301900 (NBTXR3), Cetuximab |
| NCT07075510 Subcutaneous Daratumumab Administration in the Thigh Vs Abdomen in Plasma Cell Disorders | Plasma Cell Disorder | P1P2 | Recruiting | 30 | Open-label | Daratumumab Injection |
| NCT03620903 Efficacy of First Line B-RI for Treatment Naive Waldenström's Macroglobulinemia | Waldenstrom Macroglobulinemia | P2 | Active | 53 | Open-label | Ibrutinib / Bortezomib / Rituximab |
| NCT05972135 Outpatient Administration of Teclistamab or Talquetamab for Multiple Myeloma | Multiple Myeloma | P2 | Recruiting | 100 | Open-label | Teclistamab, Talquetamab, Tocilizumab, Oral Dexamethasone |
| NCT04049669 Pediatric Trial of Indoximod With Chemotherapy and Radiation for Relapsed Brain Tumors or Newly Diagnosed DIPG | Glioblastoma, Medulloblastoma | P2 | Active | 130 | Open-label | Indoximod, Temozolomide, Cyclophosphamide, Etoposide, Lomustine |
| NCT05651945 Cardiac Rehabilitation of Stroke Survivors (SRP-CROSS) | Stroke, Cerebrovascular Accident | N/A | Recruiting | 150 | RCT, Open-label | — |
| NCT00552136 Canadian Orthopaedic Foot and Ankle Society Surgical Treatment of Ankle Arthritis Outcome Study | Ankle Arthritis | N/A | Active | 250 | RCT, Open-label | — |
| NCT07443215 Evaluation of Effect of Scatter on Visual Performance | Visual Acuity | N/A | Recruiting | 36 | RCT, Single-blind | — |
| NCT02103205 Effect of Infant Formula With Bovine Lactoferrin and Low Iron Concentration on Infant Health and Immune Function | Health of Formula-fed Children, Infant Infections in Formula-fed Children | N/A | Active | 252 | RCT, Double-blind | — |
| NCT05734638 Stress and Blood Pressure Management for Caregivers | Hypertension, Stress, Psychological | N/A | Active | 90 | RCT, Open-label | — |
| NCT06770998 A Study of a Novel EEG Neurofeedback System for PTSD Treatment | Stress Disorders, Post-Traumatic | N/A | Recruiting | 250 | RCT, Double-blind | — |
| NCT06153797 A Positive Psychology Based Intervention (PATH-C) for Caregivers of HSCT Survivors | Hematologic Malignancy, Caregiver | N/A | Active | 80 | RCT, Single-blind | — |
| NCT05256940 Motivational Interviewing to Address Suicidal Ideation for Veterans at High Risk for Suicide | Suicide, Attempted, Suicidal Ideation | N/A | Recruiting | 470 | RCT, Single-blind | — |
| NCT05903885 A Cross-sectional Partnership to Improve Prevention and Health Equity Among African Americans | Colorectal Cancer, Prevention | N/A | Recruiting | 1,200 | Single-blind | — |
| NCT02696603 Mobile Parkinson Observatory for Worldwide, Evidence-based Research (mPower) | Parkinson Disease, Neurodegenerative Diseases | N/A | Active | 20,000 | Open-label | — |
| NCT06643741 Non-Invasive Preeclampsia Screening and Biobank | Preeclampsia (PE) | Recruiting | 6,550 | — | — | |
| NCT06179758 Remote MS Care in Antwerp | Multiple Sclerosis | N/A | Active | 100 | Open-label | — |
| NCT06697093 Polish Nationwide Registry of Diagnostics, Treatment and Outcome in Patients With Cardiogenic Shock | Cardiogenic Shock | Recruiting | 500 | — | — | |
| NCT07144384 Intratumoral Injection of Standard Universal Donor Expanded Natural Killer Cells and TGF-beta Imprinted Natural Killer Cells for the Treatment of Skin Squamous Cell Carcinoma and Basal Cell Carcinoma | Skin Basal Cell Carcinoma, Skin Nodular Basal Cell Carcinoma | Early P1 | Recruiting | 40 | RCT, Open-label | Natural Killer Cell Therapy, Universal Donor Expanded TGF-beta-imprinted NK Cells |
| NCT06665295 THRIVE-CAR-T Digital App | CAR T-Cell Therapy | N/A | Recruiting | 100 | RCT, Open-label | — |
| NCT06173713 Emphasys Radiostereometric Analysis | Hip Osteoarthritis | N/A | Recruiting | 30 | Open-label | — |
| NCT04289480 Safety and Effectiveness of ENTERPRISE 2 Device in the Endovascular Treatment of Intracranial Aneurysms | Intracranial Aneurysm | Active | 164 | — | — | |
| NCT01496638 The Nordic-Baltic Bifurcation Study IV | Coronary Artery Disease | N/A | Active | 450 | RCT, Open-label | — |
| NCT06740487 Advanced Wireless Augmented Reality-Enhanced Exposure Therapy for Posttraumatic Stress Disorder | PTSD, Post Traumatic Stress Disorder | N/A | Recruiting | 40 | RCT, Open-label | — |
| NCT00299702 Evaluation of Effectiveness of Risperdal® Consta® Compared to Abilify® Over a Two-year Period in Patients With Schizophrenia | Schizophrenia, Psychotic Disorders | P4 | Completed | 355 | RCT, Open-label | Abilify, Risperidal Consta |
| NCT00236912 A Study Comparing Safety and Efficacy of Levofloxacin and Metronidazole Versus Piperacillin/Tazobactam in Treating Complicated Appendicitis | Appendicitis | P4 | Terminated | 139 | RCT, Open-label | levofloxacin; metronidazole |
| NCT00376571 Nordic Bifurcation Study. How to Use Drug Eluting Stents (DES) in Bifurcation Lesions? | Coronary Artery Disease | P4 | Completed | 413 | RCT, Open-label | — |
| NCT02065414 A Clinical Trial to Test the Effect of Experimental Mouth Rinse on Gum Disease | Gingivitis | P4 | Completed | 260 | RCT, Double-blind | — |
| NCT00086684 Effectiveness and Safety Study of Pentosan Polysulfate Sodium for the Treatment of Interstitial Cystitis | Interstitial Cystitis | P4 | Terminated | 369 | RCT, Double-blind | Pentosan polysulfate sodium 100 mg, Placebo, Pentosan polysulfate sodium 100 mg |
| NCT03733925 A Study of Golimumab in the Treatment of Indian Participants With Active Spondyloarthropathy of Ankylosing Spondylitis or Psoriatic Arthritis | Spondylitis, Ankylosing, Arthritis, Psoriatic | P4 | Completed | 100 | Open-label | Golimumab |
| NCT00743080 Randomized Controlled Trial (RCT)Comparing GYNAECARE MORCELLEX Versus ROTOCUT GI Tissue Morcellators | Uterine Myomas | P4 | Completed | — | RCT, Single-blind | — |
| NCT00219466 Clinical Study to Evaluate the Efficacy and Safety of Two Marketed Investigational Products in Children With Diaper Rash | Diaper Rash | P4 | Completed | 112 | RCT, Double-blind | — |
| NCT06044090 Brain and Stress Study | Stress, Psychological, Motivation | P4 | Completed | 10 | RCT, Double-blind | Minocycline, Placebo |
| NCT04288778 A Study to Assess Safety of Canagliflozin and Metformin Hydrochloride Combination Given as a Supplement to Diet and Exercise to Improve Blood Sugar Level in Indian Adult Participants With Diabetes | Diabetes Mellitus | P4 | Completed | 276 | Open-label | Canagliflozin + Metformin hydrochloride (Fixed Dose Combination) |
| NCT00178672 A Single Center of Carotid Stenting With Distal Protection for the Treatment of Obstructive Carotid Artery Disease | Heart Disease, Brain Vascular Accident | P4 | Completed | 69 | Open-label | — |
| NCT00194324 Effect of Exercise on Spread of the Miconozole Nitrate OVULE in the Vagina | Health, Vulvovaginal Candidiasis | P4 | Completed | 12 | RCT, Open-label | Miconazole nitrate |
| NCT00576173 An Open Label Study to Evaluate Safety, Tolerability and Clinical Utility of ULTRACET® (37.5mg Tramadol Hydrochloride/325mg Acetaminophen) for the Treatment of Breakthrough Pain in Cancer Patients | Pain | P4 | Completed | 60 | Open-label | tramadol hydrochloride; acetaminophen |
| NCT00261560 A Safety and Effectiveness Study of Acetaminophen Extended Release (3900 mg/Day) and Ibuprofen (1200 mg/Day) in the Treatment of Pain Associated With Ankle Sprains. | Sprains and Strains, Pain | P4 | Completed | 260 | RCT, Double-blind | acetaminophen |
| NCT02075528 Early Prediction of Clinical Response in Patients With Schizophrenia Treated by Paliperidone ER | Schizophrenia, Schizoaffective Disorder | P4 | Completed | 41 | Open-label | Paliperidone ER |
| NCT02932774 Randomized, Double Blind, Parallel Group, Placebo Controlled, Multi-Center Study of the Efficacy and Safety of Cetirizine HCl Syrup vs. Loratadine Syrup vs. Placebo in Treatment of Children With Seasonal Allergic Rhinitis (SAR) | Allergic Rhinitis, Hay Fever | P4 | Completed | 683 | RCT, Double-blind | Cetirizine, Loratadine |
| NCT05120141 A Twelve Week Study of Experimental Mouth Rinses | Gingivitis, Plaque | P4 | Completed | 300 | RCT, Double-blind | — |
| NCT00766402 An Efficacy and Safety Study of Tramadol/Acetaminophen Versus Diclofenac in the Treatment of Pain in Participants With Ankylosing Spondylitis Receiving Stable Treatment of Disease Modifying Anti-rheumatic Drugs (DMARDs) | Spondylitis, Ankylosing, Pain | P4 | Terminated | 8 | RCT, Open-label | Tramadol /acetaminophen, Diclofenac |
| NCT01577186 Symptomatic Remission and Social Function in Participants Treated With Paliperidone Extended Release (ER) | Schizophrenia | P4 | Completed | 480 | Open-label | Paliperidone ER |
| NCT02537522 Evaluation of 8.5 vs 9.0 Base Curve for 1-DAY ACUVUE(r) TruEye(r) Brand Contact Lenses | Contact Lens Base Curve (BC) Fit and Comfort | P4 | Completed | 72 | RCT, Double-blind | — |
| NCT00524043 An Efficacy and Safety Study of One Dosage of Paliperidone Extended Release (ER) in Treating Patients With Schizophrenia | Schizophrenia | P4 | Completed | 201 | RCT, Double-blind | Paliperidone ER, Placebo, Paliperidone ER |
| NCT00350519 The Safety and Effectiveness of PROCRIT (Epoetin Alfa) in Patients Undergoing Elective Major Abdominal and/or Pelvic Surgery | Hemostasis, Surgical | P4 | Terminated | 37 | RCT, Open-label | Epoetin alfa, Standard of Care |
| NCT00626613 The Relationship Between Risperdal Treatment and Quality of Life in Patients With Alzheimer's Disease and Behavioural and Psychological Symptoms of Dementia (BPSD) | Dementia, Alzheimer's Disease | P4 | Unknown | — | Double-blind | Risperdal,reminyl |
| NCT00385983 Total Thyroidectomy With Harmonic Scalpel® | Thyroid Neoplasm, Goiter | P4 | Unknown | 280 | RCT, Single-blind | — |
| NCT00758160 The Impact of Osmotic Release Oral Delivery System Methylphenidate (OROS MPH) Upon Family of Children and Adolescents With Attention Deficit Hyperactivity Disorder (ADHD) | Attention Deficit Disorder With Hyperactivity | P4 | Completed | 296 | Open-label | OROS Methylphenidate |
| NCT01577160 A Study to Evaluate Flexible Dose of Paliperidone Extended Release (ER) and Clinical Response in Participants With Schizophrenia | Schizophrenia | P4 | Completed | 353 | Open-label | Paliperidone ER |
| NCT07354217 Workflow Optimization During Pulse Field Ablation for Atrial Fibrillation | Pulsed Field Ablation, Lidocaine | P4 | Not Yet Recruiting | 60 | RCT, Single-blind | lidocaine, Saline |
| NCT00288535 Treatment of Bifurcated Coronary Lesions With Cypher™-Stent | Coronary Artery Disease | P4 | Unknown | 200 | RCT, Open-label | — |
| NCT00082095 To Compare Treatment With Doxorubicin or Capecitabine for Metastatic Breast Cancer in Women 60 Years and Older | Metastatic Breast Cancer | P3 | Terminated | 62 | RCT, Open-label | Pegylated liposomal doxorubicin, Capecitabine |
| NCT00097981 A Study of Thalidomide Plus Dexamethasone (Thal-Dex) Versus DOXIL plusThalidomide Plus Dexamethasone (DOXIL -Thal-Dex) in Patients With Newly Diagnosed Multiple Myeloma | Multiple Myeloma | P3 | Completed | 225 | RCT, Open-label | Thalidomide, Dexamethasone, DOXIL |
| NCT00249236 A Study of the Effectiveness and Safety of Risperidone Versus Placebo in the Treatment of Manic or Mixed Episodes Associated With Bipolar I Disorder | Bipolar Disorder, Manic Episode | P3 | Completed | 291 | RCT, Double-blind | Risperidone, oral tablets |
| NCT00210613 A Study of Withdrawal Effects With Dapoxetine in the Treatment of Premature Ejaculation | Sexual Dysfunction, Ejaculation | P3 | Completed | 199 | RCT, Double-blind | Dapoxetine |
| NCT01801436 A Post-Approval Pharmacokinetic Study of Bortezomib in Participants With Multiple Myeloma | Multiple Myeloma | P3 | Completed | 14 | Open-label | Bortezomib |
| NCT00284167 Efficacy of a Web-based Tailored Weight Management Program | Obesity | P2P3 | Completed | 1,848 | RCT, Single-blind | — |
| NCT00604630 Multicenter Efficacy Study of Recombinant Human Erythropoietin in Acute Ischemic Stroke | Infarction, Middle Cerebral Artery, Middle Cerebral Artery Stroke | P2P3 | Completed | 522 | RCT, Double-blind | recombinant human erythropoietin alfa, 0.9% NaCl |
| NCT01173562 A Safety Study of Mebendazole in Children 2 to 10 Years of Age | Healthy Volunteers | P3 | Completed | 397 | Open-label | Mebendazole |
| NCT00231634 A Study of the Efficacy and Safety of Topiramate in Obese, Type 2 Diabetic Patients Inadequately Controlled on Sulfonylurea Therapy | Obesity, Diabetes Mellitus, Type 2 | P3 | Terminated | 31 | RCT, Double-blind | topiramate |
| NCT00594516 Study on the Safety and Effectiveness of Switching Between Two Forms of Tapentadol in Patients With Chronic Low Back Pain | Low Back Pain | P3 | Completed | 117 | RCT, Double-blind | tapentadol (CG5503) Immediate Release IR, tapentadol (CG5503) Extended Release (ER), tapentadol (CG5503) Immediate Release (IR) |
| NCT00397033 Evaluation of Effectiveness and Safety of Paliperidone Extended Release in Patients With Schizoaffective Disorder. | Schizoaffective Disorder, Psychotic Disorder | P3 | Completed | 316 | RCT, Double-blind | Paliperidone ER, Paliperidone ER, Placebo |
| NCT00236509 A Study of the Efficacy and Safety of Topiramate in the Prevention of Migraine | Migraine, Common Migraine | P3 | Completed | 763 | RCT, Double-blind | topiramate |
| NCT02660372 Efficacy and Safety of Two Simeticone Brands in Adults With Functional Dyspepsia | Functional Dyspepsia | P3 | Completed | 210 | RCT, Single-blind | Imonogas, Espumisan |
| NCT00271466 A Study to Assess the Safety, Dose Conversion, and Dose Individualization of Duragesic® (Fentanyl Transdermal Patch) in the Treatment of Children With Chronic Pain Requiring Narcotic Pain Relief Therapy | Chronic Pain | P3 | Completed | 199 | Open-label | Duragesic® (fentanyl) Therapeutic Transdermal System (TTS) |
| NCT00210860 An Open Label Extension of a Study Comparing Topiramate and Amitriptyline in Migraine Prevention. | Migraine | P3 | Completed | 142 | Open-label | topiramate |
| NCT00236587 A Long Term Study of Long-acting Injectable Risperidone in the Treatment of Patients With Schizophrenia | Schizophrenia | P3 | Completed | 100 | Open-label | risperidone |
| NCT00083434 Treatment of Anemic Patients With Cancer Who Are Not Receiving Chemotherapy or Radiotherapy | Anemia, Cancer | P3 | Terminated | — | — | Epoetin alfa |
| NCT00449176 A Study to Evaluate the Effectiveness and Safety of Tapentadol (CG5503) Extended Release (ER) in Patients With Moderate to Severe Chronic Low Back Pain | Low Back Pain | P3 | Completed | 981 | RCT, Double-blind | tapentadol (CG5503) ER, oxycodone CR, placebo |
| NCT00787891 A Study of the Safety and Effectiveness of Rabeprazole for the Treatment of Gastroesophageal Reflux Disease (GERD) in Pediatric Patients | Gastroesophageal Reflux Disease (GERD) | P3 | Completed | 127 | RCT, Double-blind | rabeprazole, rabeprazole |
| NCT00229021 Doripenem in the Treatment of Complicated Lower Urinary Tract Infection or Pyelonephritis | Urinary Tract Infections, Pyelonephritis | P3 | Completed | 741 | RCT, Double-blind | doripenum |
| NCT00236665 A Study of Efficacy and Safety of Topiramate in the Treatment of Obese Patients With Mild to Moderate Essential Hypertension | Obesity, Hypertension | P3 | Completed | 531 | RCT, Double-blind | topiramate |
| NCT00086112 Study Comparing Risperidone vs Placebo as add-on Therapy in Patients With Generalized Anxiety Disorder Who Are Sub-optimally Responding to Standard Therapy. | Anxiety Disorders | P3 | Completed | 301 | RCT, Double-blind | risperidone oral tablets |
| NCT00309725 A Cardiac Safety Study of Galantamine in the Treatment of Alzheimer's Disease. | Alzheimer's Disease | P3 | Completed | 139 | RCT, Double-blind | galantamine |
| NCT00334126 Evaluation of Effectiveness and Safety of Paliperidone ER (Extended-release) Compared With Quetiapine in Patients With Schizophrenia | Schizophrenia | P3 | Completed | 399 | RCT, Double-blind | paliperidone ER tablets, quetiapine tablets, placebo - all over encapsulated |
| NCT00270179 A Study to Evaluate the Effectiveness and Safety of Epoetin Alfa During the Period When One is Donating One's Own Blood Before Surgery. | Anemia | P3 | Completed | 17 | RCT, Double-blind | epoetin alfa |
| NCT00309686 A Study to Evaluate the Efficacy and Safety of Adjustable Doses of Extended-release (ER) Paliperidone Compared With Placebo, in Combination With Lithium or Valproate, to Treat Manic and Mixed Episodes in Patients With Bipolar I Disorder | Affective Psychosis, Bipolar, Bipolar Disorder | P3 | Completed | 300 | RCT, Double-blind | Paliperidone ER |
| NCT00796120 An Efficacy and Safety Study of Trabectedin Versus Doxorubicin-Based Chemotherapy in Participants With Translocation-Related Sarcomas (TRS) | Sarcoma | P3 | Completed | 121 | RCT, Open-label | Trabectedin, Doxorubicin, Ifosfamide |
| NCT00402688 An Effectiveness and Safety Study for Levofloxacin in Chronic Prostatitis | Prostatitis | P3 | Completed | 242 | RCT, Double-blind | levofloxacin, levofloxacin, levofloxacin |
| NCT00809965 An Efficacy and Safety Study for Rivaroxaban in Patients With Acute Coronary Syndrome | Acute Coronary Syndrome, Myocardial Infarction | P3 | Completed | 15,526 | RCT, Double-blind | Rivaroxaban 2.5 mg, Rivaroxaban 5 mg, Placebo, Standard of care |
| NCT00505414 A Study to Evaluate the Effectiveness and Safety of CG5503 (Tapentadol) in the Treatment of Chronic Tumor Related Pain Compared With Placebo and Morphine | Pain, Neoplasm | P3 | Terminated | 136 | RCT, Double-blind | Tapentadol in the Titration Phase, Morphine in the Maintenance Phase, Matching Placebo in the Maintenance Phase after Tapentadol in the Titration Phase, Tapentadol in the Maintenance Phase, Morphine in the Titration Phase |
| NCT00210730 The Duration Study | Anemia | P3 | Terminated | 2 | RCT, Open-label | epoetin alfa |
| NCT00571649 Venous Thromboembolic Event (VTE) Prophylaxis in Medically Ill Patients | Venous Thromboembolism | P3 | Completed | 8,101 | RCT, Double-blind | Rivaroxaban (Xarelto, BAY59-7939), Enoxaparin, Rivaroxaban placebo, Enoxaparin placebo |
| NCT00258089 A Study of the Safety and Effectiveness of Oral Levofloxacin Compared With Oral Ciprofloxacin in the Treatment of Complicated Urinary Tract Infections | Urinary Tract Infections, Bacteriuria | P3 | Completed | 578 | RCT, Double-blind | Levofloxacin |
| NCT00210990 Doripenem in the Treatment of Complicated Lower Urinary Tract Infection or Pyelonephritis | Urinary Tract Infections, Pyelonephritis | P3 | Completed | 403 | Open-label | doripenem |
| NCT00210717 A Study to Compare the Effectiveness and Safety of Flexibly Varied Doses of Paliperidone Palmitate and Risperidone in Treating Patients With Schizophrenia | Schizophrenia | P3 | Completed | 748 | RCT, Double-blind | paliperidone palmitate |
| NCT00236795 A Study of Efficacy and Safety With the Transdermal Contraceptive System Versus Triphasil. | Contraception, Female Contraception | P3 | Completed | 1,494 | RCT, Open-label | norelgestromin + ethinyl estradiol; triphasil. |
| NCT00439777 Oral Direct Factor Xa Inhibitor Rivaroxaban in Patients With Acute Symptomatic Pulmonary Embolism - The EINSTEIN PE Study | Pulmonary Embolism | P3 | Completed | 4,833 | RCT, Open-label | Rivaroxaban (Xarelto, BAY59-7939), Enoxaparin overlapping with and followed by VKA |
| NCT00304629 Long-term Safety and Efficacy of Galantamine in Alzheimer's Disease | Alzheimer Disease | P3 | Completed | 241 | Open-label | galantamine |
| NCT00312845 Study of VELCADE and Rituximab in Patients With Relapsed or Refractory B-cell Non-Hodgkin's Lymphoma | Non-Hodgkin's Lymphoma | P3 | Completed | 676 | RCT, Open-label | Bortezomib + Rituximab, Rituximab |
| NCT00115024 EPAT: Estrogen in the Prevention of Atherosclerosis Trial | Atherosclerosis, Postmenopause | P2P3 | Completed | 222 | RCT, Double-blind | Micronized 17B-estradiol |
| NCT00253227 A Study of the Safety and Effectiveness of a Flexible Dose of Galantamine Versus Placebo in the Treatment of Patients With Alzheimer's Disease | Alzheimer Disease, Dementia | P3 | Completed | 387 | RCT, Double-blind | galantamine hydrobromide |
| NCT00035191 A Placebo-controlled Trial to Evaluate the Safety and Efficacy of Galantamine in the Treatment of Vascular Dementia | Dementia, Vascular | P3 | Completed | 254 | RCT, Double-blind | galantamine |
| NCT03224403 Randomized, Double-Blind, Single-Dose, Efficacy and Safety Study of Test Acetaminophen Tablet in Postoperative Dental Pain | Post-operative Dental Pain | P3 | Completed | 664 | RCT, Double-blind | Test acetaminophen, Commercial acetaminophen, Commercial ibuprofen, Placebo |
| NCT00421928 Tapentadol (CG5503) | Osteoarthritis, Knee, Pain | P3 | Completed | 1,030 | RCT, Double-blind | oxycodone, placebo, tapentadol (CG5503) |
| NCT00270075 A Study to Determine the Safety and Effectiveness of Epoetin Alfa in Facilitating Self-donation of Blood Before Surgery in Patients Who Are Not Anemic and Who Will be Undergoing Orthopedic or Heart and Blood Vessel Surgery | Blood Transfusion, Blood Transfusion, Autologous | P2P3 | Completed | 80 | RCT, Double-blind | epoetin alfa |
| NCT00051753 Levofloxacin In The Treatment Of Children With Recurrent And/or Persistent Acute Otitis Media | Otitis Media | P3 | Completed | 1,643 | RCT, Open-label | levofloxacin; amoxicillin/clavulanate |
| NCT00249197 A Study of the Safety and Effectiveness of Levofloxacin Compared to Ticarcillin/Clavulanate Alone or Followed by Amoxicillin/Clavulanate in the Treatment of Complicated Skin Infections | Skin Diseases, Bacterial | P3 | Completed | 413 | RCT, Open-label | levofloxacin |
| NCT00236821 A Study to Compare the Safety and Effectiveness of 2 Doses of Levofloxacin Given for Different Time Periods in Patients With Pneumonia | Pneumonia | P3 | Completed | 530 | RCT, Double-blind | levofloxacin |
| NCT00261521 A Study of the Safety and Efficacy of Long-term Correction of Anemia With Epoetin Alfa in Early Hemodialysis Patients | Kidney Failure, Chronic, Anemia | P3 | Completed | 596 | RCT, Double-blind | epoetin alfa |
| NCT00231530 A Study of the Safety and Efficacy of Topiramate in the Treatment of Obese, Type 2 Diabetes Patients on a Controlled Diet | Obesity, Diabetes Mellitus, Type 2 | P3 | Completed | 541 | RCT, Double-blind | topiramate |
| NCT00035230 A Study on the Safety and Efficacy of Topiramate in the Treatment of Patients With Bipolar I Disorder | Bipolar Disorder | P3 | Completed | 338 | RCT, Double-blind | Topiramate |
| NCT00044681 A Study of the Effectiveness and Safety of Risperidone to Augment SSRI Therapy in Patients With Treatment-resistant Depression | Depressive Disorder, Depressive Disorder, Major | P3 | Completed | 258 | RCT, Double-blind | risperidone |
| NCT00440557 An Efficacy and Safety Study of Epoetin Alfa for Initiation and Maintenance Treatment of Patients With Anemia Associated With Chronic Kidney Disease | Anemia | P3 | Completed | 375 | RCT, Open-label | Epoetin alfa 3 times weekly /once weekly, Epoetin alfa once weekly, Epoetin alfa once every two weeks |
| NCT02208947 Consumer Engagement to Increase Advance Care Planning | Advance Care Planning | P3 | Terminated | 77 | RCT, Single-blind | — |
| NCT00240786 An Effectiveness and Safety Study of Two Doses of Acetaminophen Extended Release Caplets in the Treatment of Osteoarthritis of the Hip or Knee | Osteoarthritis | P3 | Completed | 483 | RCT, Double-blind | acetaminophen extended release |
| NCT00364247 A Study to Evaluate the Effectiveness and Safety of Tapentadol(CG5503) in the Treatment of Acute Pain From Bunionectomy Compared With Placebo Followed by a Voluntary Open Label Extension for Safety. | Arthralgia, Bunion | P3 | Completed | 602 | RCT, Double-blind | CG5503 IR;tapentadol |
| NCT00271453 A Study to Assess the Safety and Effectiveness of Durogesic (Fentanyl Transdermal Patch) in the Treatment of Children With Chronic Pain Requiring Long-term Narcotic Pain Relief Therapy | Chronic Pain | P3 | Completed | 41 | Open-label | Durogesic® (fentanyl transdermal drug delivery system) |
| NCT00229060 Doripenem in the Treatment of Complicated Intra-Abdominal Infections | Bacterial Infections and Mycoses, Appendicitis | P3 | Completed | 483 | RCT, Double-blind | doripenem |
| NCT00768508 Combined Pharmacotherapies for Alcoholism | Alcoholism | P3 | Completed | 300 | RCT, Double-blind | Ondansetron 4 ug/kg b.i.d. + Cognitive Behavioral Therapy, Naltrexone 50 mg/day + Cognitive Behavioral Therapy, Ondansetron 4 ug/kg b.i.d.+ Naltrexone 50 mg/day + Cognitive Behavioral Therapy |
| NCT03439436 A Study to Compare Two Formulations of Xylometazoline/Dexpanthenol Nasal Spray for the Treatment of Nasal Congestion. | Nasal Congestion | P3 | Completed | 140 | RCT, Double-blind | xylo+dex nasal spray (0.1 mg+5 mg/dose), Nasic |
| NCT00344422 Vincristine, DOXIL (Doxorubicin HCl Liposome Injection) and Dexamethasone vs. Vincristine, Doxorubicin, and Dexamethasone in Patients With Newly Diagnosed Multiple Myeloma | Multiple Myeloma, Myeloma | P3 | Completed | 198 | RCT, Open-label | Vincristine, DOXIL (doxorubicin HCl liposomal injection), and Dexamethasone (VDD) vs. Vincristine, Doxorubicin and Dexamethasone (VAD) |
| NCT00236886 Prospective Pilot Study on Metabolism and Weight Changes in Topiramate-Treated Epilepsy Patients | Epilepsy, Epilepsies, Partial | P3 | Completed | 49 | Open-label | topiramate |
| NCT00034788 A Study on the Efficacy and Safety of Long-Term Treatment and Re-Treatment of Lower Extremity Diabetic Ulcers With REGRANEX | Foot Ulcer, Diabetic Foot | P3 | Terminated | 84 | RCT, Double-blind | Becaplermin |
| NCT01971775 Clinical Study for Energy Based Devices in Open Gastrectomy for Gastric Cancer | Gastric Cancer | P3 | Completed | 56 | RCT, Single-blind | — |
| NCT00211133 A Study to Evaluate the Impact of Maintaining Hemoglobin Levels Using Epoetin Alfa in Patients With Metastatic Breast Cancer Receiving Chemotherapy | Anemia, Breast Neoplasms | P3 | Completed | 939 | RCT, Double-blind | epoetin alfa |
| NCT00236704 A Study of the Efficacy and Safety of Topiramate as "Add on" Treatment in Epilepsy Patients With Primary Generalized Tonic-clonic Seizures | Epilepsy, Seizures | P3 | Completed | 80 | RCT, Double-blind | topiramate |
| NCT00210704 A Study of the Effectiveness and Safety of Dapoxetine in the Treatment of Men With Premature Ejaculation | Erectile Dysfunction | P3 | Completed | 1,067 | RCT, Double-blind | Dapoxetine |
| NCT02120833 A Test to Determine the Usefulness and Safety of a Cream Used on Babies With Dry Itchy Skin | Eczema | P3 | Completed | 51 | RCT, Double-blind | Colloidal Oatmeal Cream |
| NCT01226459 Clinical Trial in Females for Female Pattern Hair Loss | Androgenetic Alopecia | P3 | Completed | 404 | RCT, Double-blind | 5% Minoxidil Topical Foam, Vehicle Topical Foam |
| NCT00083668 Trial Evaluating Three Fixed Doses of Paliperidone Extended-Release (ER) Tablets and Olanzapine in the Treatment of Patients With Schizophrenia | Schizophrenia | P3 | Completed | 619 | RCT, Double-blind | Paliperidone ER |
| NCT00752427 24-Week Open Label Extension to a Randomized, 6-Week Double Blind, Placebo Controlled Study, to Evaluate the Safety and Tolerability of Flexible Doses of Extended Release OROS® Paliperidone in the Treatment of Geriatric Subjects With Schizophrenia | Schizophrenia | P3 | Completed | 86 | Open-label | Paliperidone ER OROS® |
| NCT00236444 A Study of the Efficacy and Safety of Risperidone in the Prevention of Relapse in Children and Adolescents With Conduct and Other Disruptive Behavior Disorders | Attention Deficit and Disruptive Behavior Disorders | P3 | Completed | 375 | RCT, Double-blind | risperidone |
| NCT00487435 An Open-label Extension Study With Flexible Dosing of Extended-release (ER) Tapentadol (CG5503) to Treat Patients With Moderate to Severe Chronic Pain | Pain, Osteoarthritis | P3 | Completed | 1,166 | Open-label | Tapentadol (CG5503) Extended Release (ER) |
| NCT00253188 A Study of the Safety and Effectiveness of Two Doses of Galantamine Versus Placebo in the Treatment of Patients With Alzheimer's Disease | Alzheimer Disease, Dementia | P3 | Completed | 653 | RCT, Double-blind | galantamine hydrobromide |
| NCT00034749 The Efficacy and Safety of Risperidone in the Treatment of Adolescents With Schizophrenia | Schizophrenia | P3 | Completed | 279 | RCT, Double-blind | Risperidone |
| NCT00299715 A Study to Evaluate the Efficacy and Safety of Three Fixed Doses of Extended-release Paliperidone in Subjects With Bipolar I Disorder | Bipolar Disorder, Mood Disorders | P3 | Completed | 473 | RCT, Double-blind | Paliperidone extended-release |
| NCT00236743 A Study of the Effectiveness and Safety of Topiramate in the Treatment of Children With Epilepsy | Epilepsy, Epilepsies, Partial | P3 | Completed | 90 | RCT, Double-blind | topiramate |
| NCT00270062 A Study to Evaluate the Safety of Epoetin Alfa and Its Effectiveness in Facilitating the Presurgical Collection of Blood From Anemic Patients for Possible Self-transfusion During and After Scheduled Joint Surgery. | Anemia | P3 | Completed | 77 | RCT, Double-blind | epoetin alfa |
| NCT00856596 Once a Day Topical Treatment for Athlete's Foot Fungus Inbetween the Toes in Males and Females | Tinea Pedis, Athlete's Foot | P3 | Unknown | 30 | Open-label | Sertaconazole nitrate cream 2% |
| NCT00236873 A Study of the Efficacy and Safety of Topiramate as add-on Therapy in the Treatment of Epilepsy Patients With Difficult to Treat, Partial-onset Seizures. | Epilepsy, Epilepsies, Partial | P2 | Completed | 47 | RCT, Double-blind | topiramate |
| NCT04621500 Vitamin D Supplementation in RNA-seq Profiles of Single-core Prostate Samples, Among Veterans | Prostate Cancer, Vitamin D Deficiency | P2 | Completed | 60 | Open-label | cholecalciferol |
| NCT05612711 Dronabinol for Agitation in Dementia Crossover Trial | Dementia Moderate, Dementia Severe | P2 | Withdrawn | — | RCT, Double-blind | Dronabinol |
| NCT03330275 Evaluating the Impact of JJVC Senofilcon A - Based Contact Lens With New UV-blocker on Day and Night Driving Performance | Visual Performance | P2 | Completed | 24 | RCT, Single-blind | — |
| NCT00337935 A Study of the Use of PROCRIT (Epoetin Alfa) for the Treatment of Anemia in People With Chronic Kidney Disease Who Live in Long-term Care Facilities. | Renal Failure , Chronic, Anemia | P2 | Completed | 157 | RCT, Open-label | Epoetin Alfa |
| NCT00973141 A Dose-ranging Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Osteoarthritis-related Pain | Osteoarthritis, Osteoarthritis, Hip | P2 | Terminated | 467 | RCT, Double-blind | JNJ-42160443, JNJ-42160443, JNJ-42160443, Placebo, JNJ-42160443, JNJ-42160443 |
| NCT05660421 Itacitinib for the Treatment Steroid Refractory Immune Related Adverse Events Arising From Immune Checkpoint Inhibitors | Hematopoietic and Lymphoid Cell Neoplasm, Malignant Solid Neoplasm | P2 | Withdrawn | — | Open-label | Itacitinib, Corticosteroid |
| NCT00006205 Alcohol Dependency Study: Combining Medication Treatment for Alcoholism | Alcoholism | P2 | Unknown | 320 | RCT, Double-blind | ondansetron + cognitive behavioral therapy, topiramate + cognitive behavioral therapy, Placebo + cognitive behavioral therapy, ondansetron + topiramate + cognitive behavioral therapy |
| NCT00639860 Evaluation of OSSIX-Plus Resorbable Collagen Membranes for Alveolar Ridge Preservation Following Exodontia | Alveolar Bone Loss, Loss of Teeth Due to Extraction | P1P2 | Completed | 10 | Open-label | — |
| NCT00210574 A Pilot Study of Topiramate in Childhood Absence Epilepsy | Epilepsy, Absence | P2 | Completed | 12 | Open-label | topiramate |
| NCT00338299 Alternate Dosing of PROCRIT (Epoetin Alfa) in Patients With Cancer and Chemotherapy Induced Anemia | Anemia, Chemotherapy | P2 | Completed | 51 | Open-label | Epoetin alfa |
| NCT00236860 A Study of the Efficacy and Safety of Topiramate as add-on Therapy in the Treatment of Epilepsy Patients With Difficult to Treat, Partial-onset Seizures | Epilepsy, Epilepsies, Partial | P2 | Completed | 56 | RCT, Double-blind | topiramate |
| NCT00530166 Effectiveness and Safety Study for JNJ-18054478 in Asthma Patients. | Asthma | P2 | Terminated | 26 | RCT, Double-blind | JNJ-18054478, sham comparator |
| NCT00231647 A Study on Efficacy and Safety of Topiramate OROS Controlled-Release in Obese, Type 2 Diabetic Subjects Managed With Diet or Metformin | Obesity, Diabetes Mellitus, Type 2 | P2 | Completed | 113 | RCT, Double-blind | topiramate |
| NCT02320708 Study of Acetaminophen (ACE) in Post-operative Dental Pain | Dental Pain | P2 | Completed | 240 | RCT, Double-blind | Acetaminophen (ACE) (1000 mg), Commercial ACE (1000 mg), Commercial Ibuprofen (IBU) (400 mg), Placebo, Placebo, Placebo |
| NCT03388138 Clinical Evaluation of Etafilcon A With Ketotifen | Visual Acuity | P2 | Completed | 143 | RCT, Double-blind | — |
| NCT05517668 Evaluation of the Efficacy of Fomepizole in the Treatment of Acetaminophen Overdose | Acetaminophen, Drug Overdose | P2 | Terminated | 29 | RCT, Double-blind | Intravenous infusion of N-acetylcysteine, Intravenous infusion of Fomepizole (4-MP) |
| NCT00728195 An Efficacy and Safety Study of 3 Fixed Doses of JNJ-37822681 in Participants With Schizophrenia | Schizophrenia | P2 | Completed | 498 | RCT, Double-blind | JNJ-37822681, JNJ-37822681, JNJ-37822681, Olanzapine, Placebo |
| NCT00240812 A Study to Determine if Ibuprofen in Combination With Pseudoephedrine HCl is More Effective Than Each Drug Alone in the Treatment of Nighttime Bedwetting | Enuresis | P2 | Completed | 318 | RCT, Double-blind | ibuprofen; pseudoephedrine HCl |
| NCT00744757 An Efficacy and Safety Study of Decitabine in Participants With Myelodysplastic Syndrome (MDS) | Myelodysplastic Syndrome | P2 | Completed | 37 | Open-label | Decitabine |
| NCT00270270 A Study to Evaluate the Safety and Efficacy of Epoetin Alfa Versus Placebo for the Treatment of Anemia in AIDS (Acquired Immunodeficiency Syndrome) Patients With Anemia Caused by the Disease and by Zidovudine (AZT) Therapy | Acquired Immunodeficiency Syndrome, Anemia | P2 | Completed | 63 | RCT, Double-blind | epoetin alfa |
| NCT01060254 A Study to Evaluate the Pain Relieving Effects, Safety, and Tolerability of JNJ-42160443 for the Relief of Bladder Pain | Cystitis, Interstitial, Urologic Diseases | P2 | Terminated | 31 | RCT, Double-blind | Placebo, JNJ-42160443 |
| NCT00269945 A Study to Evaluate the Safety and Effectiveness of Epoetin Alfa in AIDS Patients With Anemia Caused Both by Their Disease and by AZT (Zidovudine, an Antiviral Drug) Given as Treatment for Their Disease | Anemia, Acquired Immunodeficiency Syndrome | P2 | Completed | 60 | RCT, Double-blind | epoetin alfa |
| NCT01075659 Early Effects of a New Oral Nicotine Replacement Product and NiQuitin™ Lozenge | Smoking Cessation | P2 | Completed | 200 | RCT, Open-label | Nicotine, Nicotine, Nicotine |
| NCT00223639 New Medications to Treat Alcohol Dependence | Alcoholism | P2 | Completed | 29 | RCT, Double-blind | Topiramate |
| NCT00072670 A Phase 2 Study of Trabectedin (Yondelis) in Adult Male Participants With Advanced Prostate Cancer | Prostate Cancer | P2 | Completed | 59 | Open-label | Trabectedin |
| NCT00786422 Deep Vein Thrombosis Treatment With the Oral Direct Factor Xa Inhibitor Rivaroxaban in Patients Using a Strong CYP 3A4 Inducer | Venous Thrombosis, Deep Vein Thrombosis | P2 | Completed | 25 | Open-label | Rivaroxaban (Xarelto, BAY59-7939) |
| NCT00063297 Safety and Efficacy of Study Drug Versus Placebo for Negative Symptoms of Schizophrenia | Schizophrenia | P2 | Completed | 180 | RCT, Double-blind | R209130 |
| NCT00641511 Pharmacogenetic Clinical Trial of Nepicastat for Post Traumatic Stress Disorder (PTSD) | Post Traumatic Stress Disorder (PTSD) | P2 | Withdrawn | — | RCT, Double-blind | SYN117 (nepicastat), Placebo comparator |
| NCT00231673 A Study To Evaluate The Effect Of Topiramate On Clinical And Electrophysiological Parameters In Subjects With Diabetic Peripheral Polyneuropathy | Diabetic Neuropathies, Diabetes Mellitus, Type 2 | P2 | Completed | 72 | RCT, Double-blind | Topiramate |
| NCT01241422 A Study to Evaluate the Effectiveness of JNJ 40929837 for the Treatment of Asthma Using a Bronchial Allergen Challenge Model | Asthma | P2 | Completed | 22 | RCT, Double-blind | JNJ 40929837, Placebo, Montelukast |
| NCT01812642 A Pharmacokinetics Study to Evaluate Safety and Tolerability of JNJ-37822681 in Participants With Stable Schizophrenia | Schizophrenia | P2 | Completed | 33 | RCT, Double-blind | JNJ-37822681 |
| NCT00515034 A Safety and Tolerability Study of Doripenem in Patients With Abdominal Infections or Pneumonia | Pneumonia, Ventilator-Associated, Pneumonia, Bacterial | P2 | Completed | 146 | RCT, Open-label | Imipenem/cilastatin, Imipenem/cilastatin, Doripenem, Doripenem |
| NCT00223626 Topiramate to Reduce Cocaine Dependence | Cocaine-Related Disorders | P2 | Completed | 25 | RCT, Double-blind | Topiramate |
| NCT01120210 A Study to Investigate the Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of an Intravenous Solution of JNJ-39588146 or Placebo in Patients With Heart Failure | Heart Failure | P2 | Completed | 62 | RCT, Double-blind | JNJ-39588146 5 ng/kg/min, JNJ-39588146 15 ng/kg/min, JNJ-39588146 30 ng/kg/min, Placebo, JNJ-39588146 5, 15, or 30 ng/kg/min |
| NCT00050440 Phase 2 Study of ET-743 (Trabectedin) in Patients With Persistent or Recurrent Endometrial Carcinoma | Endometrial Neoplasms, Uterine Neoplasms | P2 | Completed | 50 | Open-label | Trabectedin, Dexamethasone |
| NCT00579384 A Study of the Effects of JNJ-26489112 on the Photic Induced Paroxysmal Electroencephalogram (EEG) Response in Patients With Photosensitive Epilepsy | Photosensitive Epilepsy | P2 | Completed | 12 | Single-blind | JNJ-26489112, Placebo |
| NCT00604123 A Study Evaluating Effects of Intranasal JNJ-17166864 on Symptoms of Allergic Rhinitis in Adults | Allergic Rhinitis | P2 | Completed | 74 | RCT, Double-blind | JNJ-17166864, Placebo |
| NCT00050427 A Study of ET-743 (Trabectedin) in Patients With Advanced Breast Cancer | Breast Neoplasms, Neoplasms | P2 | Completed | 53 | RCT, Open-label | ET743, ET743 |
| NCT00786838 A Study to Assess the Potential Effects of a Single-Dose Administration of Trabectedin on the QT Intervals of the Electrocardiogram | Solid Tumor | P2 | Completed | 76 | Single-blind | Trabectedin, Placebo |
| NCT00337948 An Efficacy and Safety Study of PROCRIT (Epoetin Alfa) in Cancer Patients Receiving Chemotherapy Every Week or Every Four Weeks | Chemotherapy, Anemia | P2 | Completed | 129 | Open-label | Epoetin alfa |
| NCT00566202 A Safety and Effectiveness Study of JNJ-18038683 in Patients With Moderate to Severe Depression | Major Depressive Disorder | P2 | Completed | 67 | RCT, Double-blind | Placebo, Escitalopram, JNJ-18038683 |
| NCT00548275 Reducing Sex-Related HIV Risk Behaviors in Patients Receiving Treatment for Opioid Dependence | Opiate Dependence, HIV Infections | P2 | Completed | 22 | RCT, Open-label | — |
| NCT00706953 A Study of Bortezomib and Pegylated Liposomal Doxorubicin in Patients With Relapsed Multiple Myeloma Previously Treated With Bortezomib | Multiple Myeloma | P2 | Withdrawn | — | Open-label | bortezomib; pegylated liposomal doxorubicin |
| NCT00212875 A Study of Four Dosing Regimens of PROCRIT (Epoetin Alfa) in Patients With Chronic Kidney Disease. Protocol Addendum: Extension Study of Maintenance Therapy of PROCRIT (Epoetin Alfa) in Patients With Chronic Kidney Disease. | Chronic Kidney Disease, Anemia | P2 | Completed | 267 | RCT, Open-label | epoetin alfa |
| NCT00973024 A Dose-ranging Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Low Back Pain | Low Back Pain, Low Back Pain, Recurrent | P2 | Terminated | 389 | RCT, Double-blind | JNJ-42160443 3 mg, JNJ-42160443 1 mg, JNJ-42160443 6 mg/3mg, JNJ-42160443 10 mg, Matching Placebo |
| NCT02691507 Trial to Determine the Therapeutic Benefit of an OTC Cream on Dry, Itchy Skin of Adults and Children With Eczema | Atopic Dermatitis | P2 | Completed | 53 | RCT, Double-blind | Experimental Product 1% Colloidal Oatmeal Balm |
| NCT00388635 Velcade-Melphalan-Prednisone in Older Untreated Multiple Myeloma Patients. | Multiple Myeloma | P1P2 | Completed | 60 | Open-label | Velcade, Melphalan, Prednisone |
| NCT00880217 A Study to Evaluate 3 Different Doses of JNJ-31001074 in the Treatment of Adults With Attention-Deficit/Hyperactivity Disorder (ADHD) | Attention Deficit Hyperactivity Disorder | P2 | Completed | 430 | RCT, Double-blind | Atomoxetine 80 mg/d, Placebo, OROS methylphenidate HCl 54 mg/d, JNJ-31001074 3 mg/d, JNJ-31001074 1 mg/d, JNJ-31001074 10 mg/d |
| NCT01230749 A Study of Multiple Oral Doses of JNJ-41443532 in Patients With Type 2 Diabetes Mellitus | Diabetes Mellitus, Type 2 | P2 | Completed | 89 | RCT, Double-blind | JNJ-41443532, Pioglitazone 30 mg, Placebo |
| NCT01814982 An Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics Study of JNJ-17299425 in Participants With Traumatic Brain Injury | Traumatic Brain Injury | P2 | Terminated | 7 | Open-label | JNJ-17299425 |
| NCT00269997 A Study to Evaluate the Safety and Effectiveness of Epoetin Alfa Versus Placebo in Patients With Persistent Anemia as a Result of Cancer Treatment With Cisplatin, a Platinum-containing Chemotherapy Drug | Anemia, Neoplasms | P2 | Completed | 72 | RCT, Double-blind | epoetin alfa |
| NCT00228995 A Phase II Study to Assess Changes in Physical Function in Elderly Patients With Chronic Anemia | Anemia, Aged | P2 | Terminated | 9 | RCT, Double-blind | epoetin alfa |
| NCT00871507 A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (Explores What the Body Does to the Drug), and Pharmacodynamics (Explores What a Drug Does to the Body) of JNJ-38431055 in Volunteers With Type 2 Diabetes Mellitus | Diabetes Mellitus, Type 2 | P1 | Completed | 25 | RCT, Double-blind | JNJ-38431055 Dose 1, Sitagliptin 100 mg, Placebo, JNJ-38431055 Dose 2 |
| NCT01273506 A Study to Compare the Bioequivalence of 50-mg Tapentadol (CG5503) Dose Administered as Two 25-mg Tablets Relative to One 50-mg Tablet | Healthy Volunteer | P1 | Completed | 30 | RCT, Open-label | tapentadol (CG5503) ER 25-mg TRF, tapentadol (CG5503) ER 50-mg TRF |
| NCT00791349 A Study of QT and QTc Intervals in Patients Administered Immediate Release Paliperidone | Schizophrenia, Schizoaffective Disorder | P1 | Completed | 141 | RCT, Double-blind | Immediate release (IR) Paliperidone |
| NCT01787357 A Study to Assess Electrocardiogram Results in Healthy Volunteers Receiving Canagliflozin (JNJ-28431754) | Healthy | P1 | Completed | 60 | RCT, Double-blind | Canagliflozin (JNJ-28431754), Placebo, Moxifloxacin |
| NCT00269009 CHERL, Connecting Primary Care Patients With Community Resources to Facilitate Behavior Change | Tobacco Use Disorder, Alcohol Abuse | P1 | Unknown | — | RCT, Double-blind | — |
| NCT00838669 A Study of the Effect of Food and Posture on the Pharmacokinetics of a Single Dose of ER OROS Paliperidone | Schizophrenia | P1 | Completed | 74 | RCT, Open-label | Extended release OROS paliperidone |
| NCT01173549 A Study of 28431754 (Canagliflozin) on Gastrointestinal Glucose Absorption and Metabolism in Healthy Volunteers | Healthy | P1 | Completed | 26 | RCT, Double-blind | Canagliflozin/Placebo Placebo/Canagliflozin |
| NCT04921371 Six Week Study of Experimental Mouth Rinses: Effect on Gingivitis and Plaque | Gingivitis, Plaque | P1 | Completed | 157 | RCT, Double-blind | — |
| NCT00040105 Zarnestra and Gleevec in Chronic Phase Chronic Myelogenous Leukemia | Leukemia, Myeloid, Chronic | P1 | Completed | 26 | Open-label | Zarnestra (R115777), Gleevec (Imatinib mesylate) |
| NCT00967070 Skin Sensitization Potential of a New Nicotine Patch | Smoking Cessation | P1 | Completed | 257 | RCT, Double-blind | Nicotine Patch, Placebo Patch |
| NCT01026636 A Single-Dose Pharmacokinetics and Safety Study of Ceftobiprole in Pediatric Patients =3 Months to <18 Years of Age | Staphylococcal Skin Infections, Streptococcal Infections | P1 | Completed | 64 | Open-label | Ceftobiprole |
| NCT01733108 A Study to Assess the Effects of Canagliflozin (JNJ-28431754) on the Pharmacokinetics, Pharmacodynamics, and Safety of Glyburide in Healthy Volunteers | Healthy | P1 | Completed | 29 | Open-label | Glyburide, Canagliflozin (JNJ-28431754) |
| NCT01358006 A Dose-Ranging Study of JNJ-40411813 in Healthy Male Volunteers | Healthy | P1 | Completed | 13 | Open-label | JNJ-40411813, JNJ-40411813 |
| NCT00790777 A Study of the Bioequivalence of 12 mg Paliperidone Extended Release Tablets Manufactured at Gurabo and Vacaville | Schizophrenia | P1 | Completed | 72 | RCT, Open-label | Paliperidone ER |
| NCT01518712 A Study to Assess the Bioequivalence of 2 Fixed Dose Combination (FDC) Tablets of Canagliflozin and Metformin Immediate Release (IR) (150 mg/850 mg) With Respect to the Individual Components of Canagliflozin (1 x 300 mg) and Metformin IR Tablets (2 x 850 mg) in Healthy Volunteers | Healthy | P1 | Completed | 64 | RCT, Open-label | A (canagliflozin and metformin IR individual tablets) / B (canagliflozin/metformin IR FDC tablets), B (canagliflozin/metformin IR FDC tablets / A (canagliflozin and metformin IR individual tablets) |
| NCT00791713 A Study of the Effects of Paroxetine on the Pharmacokinetics of Paliperidone ER | Schizophrenia | P1 | Completed | 60 | RCT, Open-label | Paliperidone ER |
| NCT01454622 A Study to Assess the Bioequivalence of 2 Fixed Dose Combination (FDC) Tablets of Canagliflozin and Metformin Immediate Release (IR) (50 mg/1,000 mg) With Respect to the Individual Components of Canagliflozin (1 x 100 mg) and Metformin IR Tablets (2 x 1,000 mg) in Healthy Volunteers | Healthy | P1 | Completed | 64 | RCT, Open-label | A (canagliflozin and metformin IR individual tablets) / B (canagliflozin/metformin IR FDC tablets), B (canagliflozin/metformin IR FDC tablets / A (canagliflozin and metformin IR individual tablets) |
| NCT01054352 A Single and Multiple Dose Study to Explore the Safety of JNJ-38224342 in Healthy Patients and Patients With Seasonal Allergies | Seasonal Allergic Rhinitis | P1 | Completed | 182 | RCT, Double-blind | JNJ38224342, JNJ38224342/placebo, JNJ38224342/placebo, JNJ38224342/placebo |
| NCT03979989 Drug-drug Interaction Study to Evaluate the Effect of Omeprazole on CG5503 (Tapentadol) | Pharmacokinetic | P1 | Completed | 32 | RCT, Open-label | Tapentadol IR capsule, Omeprazole capsule |
| NCT01556217 A Pharmacokinetic Study to Characterize JNJ-39393406 in the Cerebrospinal Fluid of Healthy Volunteers | Healthy Volunteers | P1 | Completed | 12 | RCT, Double-blind | JNJ-39393406, Placebo |
| NCT00791193 A Pharmacokinetic Study of the Relative Bioavailability of Paliperidone ER Formulations With Different Release Profiles and a Comparison to Paliperidone IR | Schizophrenia | P1 | Completed | 80 | RCT, Open-label | Paliperidone ER |
| NCT00601432 A Study to Evaluate the Effect of Food on Levofloxacin Pharmacokinetics From an Oral Solution Formulation | Healthy | P1 | Completed | 24 | RCT, Open-label | levofloxacin oral solution |
| NCT00456170 Are Sutures Required for Vaginal Hysterectomy: A Randomized Controlled Trial | Vaginal Hysterectomy | P1 | Unknown | 60 | RCT, Open-label | — |
| NCT00796185 As Study of the Pharmacokinetics of Paliperidone Extended-release and Risperidone Immediate-release Formulations | Schizophrenia, Schizoaffective Disorder | P1 | Completed | 62 | RCT, Open-label | Paliperidone ER |
| NCT02019485 A Study to Assess Bioequivalence of a New Tapentadol Extended-Release Tablet With Respect to a Tapentadol Extended Release Tablet Under Fasted Conditions in Healthy Subjects | Healthy | P1 | Completed | 64 | RCT, Open-label | Tapentadol Extended Release (ER) Tamper-Resistant Formulation (TRF), Tapentadol Prolonged-Release Formulation 2 (PR2) |
| NCT05182047 A Study of Butamirate Citrate Syrup Versus (vs) Sinecod Syrup (Vanilla) in Adult Healthy Study Volunteers | Healthy | P1 | Withdrawn | — | RCT, Open-label | Butamirate citrate, Sinecod |
| NCT00762749 Study to Evaluate Diphenhydramine in Children and Adolescents | Allergic Rhinitis | P1 | Completed | 36 | Open-label | diphenhydramine HCl |
| NCT01273558 A Study of Two Methods for Determining the Renal Threshold for Glucose in Patients With Type 2 Diabetes Mellitus | Diabetes Mellitus, Type 2 | P1 | Completed | 28 | Open-label | Canagliflozin |
| NCT00676910 A Research Study of JNJ-26854165 to Determine the Safety and Dose in Patients With Advanced Stage or Refractory Solid Tumors. | Neoplasms | P1 | Completed | 71 | Open-label | JNJ-26854165 |
| NCT00967174 Cumulative Skin Irritation Potential of a New 25 mg Nicotine Patch | Smoking Cessation | P1 | Completed | 42 | RCT, Double-blind | Nicotine Patch, Placebo Patch, SLS Comparator Patch |
| NCT02049697 A Study to Evaluate of the Absorption, Metabolism, and Excretion of 14C-JNJ-39823277 in Healthy Male Participants | Healthy | P1 | Completed | 6 | Open-label | 14C-JNJ-39823277 |
| NCT01294631 A Pharmacodynamics, Pharmacokinetics, and Safety Study of Hydrochlorothiazide and Canagliflozin in Healthy Volunteers | Healthy | P1 | Completed | 30 | Open-label | Canagliflozin 300 mg once daily and HCTZ 25 mg once daily |
| NCT01128985 A Pharmacokinetic and Pharmacodynamic Study to Determine Blood Levels of JNJ-28431754 (Canagliflozin) in Patients With Type 2 Diabetes Mellitus | Diabetes Mellitus, Type 2 | P1 | Completed | 39 | RCT, Double-blind | Canagliflozin 50 mg, Canagliflozin 100 mg, Canagliflozin 300 mg, Placebo |
| NCT01586507 A Study of ULTRAM ER at Two Dose Levels in Adolescents With Pain | Pain | P1 | Completed | 38 | Open-label | ULTRAM ER, ULTRAM ER |
| NCT01428284 A Study to Assess the Effects of Multiple-Dose Probenecid on the Multiple-Dose Pharmacokinetics of Canagliflozin in Healthy Volunteers | Healthy | P1 | Completed | 14 | Open-label | Canagliflozin/Probenecid |
| NCT00892541 A Study of the Potential Effects of Trimethoprim on the Pharmacokinetics of ER OROS Paliperidone | Schizophrenia | P1 | Completed | 30 | RCT, Open-label | ER OROS paliperidone |
| NCT00762567 Phenylephrine Pediatric Pharmacokinetic Study | Rhinitis | P1 | Completed | 36 | Open-label | phenylephrine HCl |
| NCT04186936 A Study of Combination Caplet With Loperamide Hydrochloride and Simethicone, and Imodium Express Tablets-lyophilizate Coadministered With Espumisan Capsule in Healthy Volunteers | Healthy | P1 | Completed | 48 | RCT, Open-label | Combination Caplet with Loperamide HCl and Simethicone, Loperamide HCl, Simethicone |
| NCT00921154 Ivermectin Solution Bioequivalence Study - Fasted | Healthy | P1 | Completed | 24 | RCT, Open-label | ivermectin |
| NCT07180420 Proof of Concept (PoC) Evaluation of Naloxone Unique Intramuscular (IM) Injection | Healthy Volunteer - Complete | P1 | Completed | 12 | Open-label | naloxone IM |
| NCT00965913 Cumulative Skin Irritation Potential of a New 15 mg Nicotine Patch | Smoking Cessation | P1 | Completed | 42 | RCT, Double-blind | Nicotine Patch, Nicotine Patch Comparator, Placebo Patch |
| NCT01981278 A Study to Assess Bioequivalence of a New Tapentadol Extended-Release 250-mg Tablet With Respect to a Tapentadol Extended-Release 250-mg Tablet in Healthy Participants | Healthy | P1 | Completed | 63 | RCT, Open-label | Tapentadol ER 250-mg TRF tablet, Tapentadol ER 250-mg PR2 tablet |
| NCT01756404 Study to Assess the Pharmacokinetics, Pharmacodynamics, and Safety of Canagliflozin (JNJ-28431754) in Otherwise Healthy Obese Volunteers | Healthy | P1 | Completed | 80 | RCT, Double-blind | Canagliflozin (JNJ-28431754), Placebo |
| NCT01748526 A Study to Assess the Pharmacokinetics and Pharmacodynamics of Canagliflozin (JNJ-28431754) in Healthy Indian Volunteers | Healthy | P1 | Completed | 16 | RCT, Open-label | Canagliflozin (JNJ-28431754) 200 mg, Canagliflozin (JNJ-28431754) 300 mg |
| NCT00676299 A Safety and Dose-finding Study of JNJ-26483327, a Drug in Development for Cancer, for Patients With Advanced and/or Refractory Solid Malignancies. | Protein Kinase Inhibitors, Antineoplastic Protocols | P1 | Completed | 19 | Open-label | JNJ-26483327 |
| NCT01157000 A Pharmacokinetic and Bioavailability Study of 28431754 (Canagliflozin) in Healthy Male Volunteers | Healthy | P1 | Completed | 9 | Open-label | Canagliflozin |
| NCT00796471 A Pharmacokinetics and Pharmacodynamics Study Under Fasting and Fed Conditions With Paliperidone Extended-release and Immediate-release Formulations | Schizophrenia | P1 | Completed | 35 | RCT, Open-label | Paliperidone ER |
| NCT05844995 A Study of Acetaminophen/Naproxen Sodium Fixed Combination Tablets in Adolescents 12 to <17 Years of Age With Pain | Orthodontic Pain | P1 | Completed | 24 | Open-label | Acetaminophen/Naproxen Sodium |
| NCT00608907 An Open-Label Study to Assess the Effect of CYP3A4 Induction on the Pharmacokinetics of VELCADE (Bortezomib) | Multiple Myeloma, Non-Hodgkin's Lymphoma | P1 | Completed | 61 | RCT, Open-label | bortezomib, bortezomib, rifampicin, bortezomib, dexamethasone |
| NCT01932333 A Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of JNJ-40411813 in Male and Female Elderly Patients | Healthy | P1 | Completed | 36 | RCT, Double-blind | JNJ-40411813 50 mg, JNJ-40411813 100 mg, Placebo |
| NCT00769158 Combining Medications for the Treatment of Alcohol Dependence: An Inpatient Preliminary Study | Alcoholism | P1 | Completed | 4 | RCT, Double-blind | Topiramate and Naltrexone |
| NCT00258063 A Study to Evaluate the Exposure of Norelgestromin and Ethinyl Estradiol From Commercial Lots of EVRA (a Transdermal Contraceptive Patch Manufactured by LOHMANN Therapie-Systeme) and CILEST (an Oral Contraceptive) | Contraception, Female Contraception | P1 | Completed | 60 | RCT, Open-label | EVRA® transdermal contraceptive patch containing 6 mg of norelgestromin and 0.60 mg of ethinyl estradiol (versus CILEST® tablets). |
| NCT00602589 A Study to Evaluate the Bioequivalence of an Oral Suspension Formulation, an Oral Solution Formulation, and the Marketed Tablet Formulation of Levofloxacin in Healthy Subjects | Healthy | P1 | Completed | 72 | RCT, Open-label | Levofloxacin oral suspension; Levofloxacin oral solution; and Levofloxacin marketed tablet formulations |
| NCT00796081 A Safety and Pharmacokinetic Study of ER OROS Paliperidone in Pediatric Patients With Schizophrenia, Schizoaffective Disorder, or Schizophreniform Disorder | Schizophrenia, Schizoaffective Disorder | P1 | Completed | 25 | RCT, Open-label | ER OROS paliperidone, paliperidone ER |
| NCT01487512 Effect of Dose on the Pharmacokinetics of OROS Hydromorphone Under Fasted Conditions in Healthy Taiwanese Participants | Healthy Volunteers | P1 | Completed | 29 | RCT, Open-label | Treatment A: Hydromorphone 8 mg, Treatment B: Hydromorphone 16 mg, Treatment C: Hydromorphone 32 mg, Treatment D: Hydromorphone 64 mg |
| NCT00709267 Bioavailability Study of Folic Acid in Healthy Women | Healthy, Pharmacokinetics | P1 | Completed | 12 | RCT, Open-label | Folic acid |
| NCT00791622 A Study of QT and QTc Intervals in Patients Administered Extended Release Paliperidone or Quetiapine | Schizophrenia, Schizoaffective Disorder | P1 | Completed | 110 | RCT, Double-blind | Paliperidone ER |
| NCT00796029 A Study of Plasma Concentrations, Metabolism and Excretion of 14C-paliperidone After a Single Oral Dose | Schizophrenia | P1 | Completed | 5 | Open-label | 14C-paliperidone |
| NCT00915434 A Study to Characterize the Pharmacokinetics and Effect of Food on JNJ-31001074 in Healthy Volunteers | Healthy, Pharmacokinetics | P1 | Completed | 20 | RCT, Open-label | JNJ-31001074 |
| NCT00102609 A Safety Study Utilizing Yondelis and Doxorubicin in Patients With a Type of Cancer Called Soft Tissue Sarcoma | Soft Tissue Sarcoma, Sarcoma | P1 | Completed | 41 | Open-label | Doxorubicin, Trabectedin, Dexamethasone |
| NCT01186497 A Relative Bioavailability Study of Rabeprazole Sodium Administered With Different Dosing Vehicles in Healthy Adult Volunteers | Healthy | P1 | Completed | 35 | RCT, Open-label | Rabeprazole sodium: Treatment E, Rabeprazole sodium: Treatment C, Rabeprazole sodium: Treatment D, Rabeprazole sodium: Treatment A, Rabeprazole sodium: Treatment B |
| NCT00892320 A Study of the Effect of Food on the Pharmacokinetics of ER OROS Paliperidone in Healthy Japanese Volunteers | Schizophrenia | P1 | Completed | 20 | RCT, Open-label | ER OROS paliperidone |
| NCT03130179 A Bioequivalence Study Between Two Nicotine Replacement Therapies in Adult Healthy Smokers Motivated to Quit. | Tobacco Dependence | P1 | Completed | 244 | RCT, Open-label | Nicorette Strongmint lozenge 4 mg, Niquitin MiniMint lozenge 4 mg |
| NCT00796835 A Dose-proportionality Study of Five Tablet Strengths of ER OROS Paliperidone | Schizophrenia | P1 | Completed | 50 | RCT, Open-label | ER OROS Paliperidone |
| NCT00258076 A Study to Evaluate the Hormone Exposure From Multiple Commercial Lots of ORTHO EVRA (a Transdermal Contraceptive Patch) | Contraception, Female Contraception | P1 | Completed | 53 | RCT, Open-label | EVRA transdermal contraceptive patch 6 mg NGMN and 0.75 mg EE |
| NCT01555476 Study to Test the Blood to See if a New Medicine is Likely to Provide Pain Relief Similar to a Product Already Sold in Stores | Pain | P1 | Completed | 32 | RCT, Open-label | Ibuprofen, Ibuprofen |
| NCT01094249 A Drug Interaction Study of Valproic Acid and Paliperidone Extended-Release (ER) in Patients With Schizophrenia, Bipolar I Disorder, or Schizoaffective Disorder | Schizophrenia, Bipolar Disorder | P1 | Completed | 9 | Open-label | divalproex sodium ER/paliperidone ER |
| NCT01316978 A Study to Test Bioequivalence Between One Test Formulation of Ibuprofen and Two Reference Treatments | Pain | P1 | Completed | 30 | RCT, Single-blind | Ibuprofen, Ibuprofen, Ibuprofen |
| NCT01177150 A First-in-Human Study of JNJ-28431754 in Healthy Male Volunteers | Healthy | P1 | Completed | 71 | RCT, Double-blind | JNJ-28431754/ Placebo, JNJ-28431754 |
| NCT00135213 PROS Brief Smoking Cessation Counseling in Pediatric Practice to Reduce Secondhand Smoke Exposure of Young Children | Health Care Quality, Access, and Evaluation, Smoking Cessation | P1 | Completed | 1,200 | RCT, Double-blind | — |
| NCT01535820 The Effect of an Adhesive Overlay on the Delivery of Contraceptive Hormones From ORTHO EVRA® in Healthy Women | Healthy Volunteers | P1 | Completed | 54 | RCT, Open-label | Treatment A: ORTHO EVRA patch (NGMN + EE) with an adhesive overlay, Treatment B: ORTHO EVRA patch (NGMN + EE) without an overlay |
| NCT04794751 Evaluation of Investigational Daily Disposable Multifocal Contact Lenses Produced With Different Manufacturing Processes | Visual Acuity | N/A | Completed | 78 | RCT, Single-blind | — |
| NCT03787212 MiBo ThermoFlo Lid Temperature Evaluation | Dry Eye | N/A | Terminated | 4 | RCT, Open-label | — |
| NCT03635528 Evaluating Accommodative Responses of Soft Contact Lenses for Myopia Control | Visual Acuity | N/A | Completed | 11 | RCT, Double-blind | — |
| NCT06767319 Prospective, Multi-center, Non-interventional, Open Label, Randomized (Depth of Focus Testing Sequences), Clinical Study | Depth of Focus | Completed | 79 | — | — | |
| NCT00234806 Health-e-Access Telemedicine in Primary Pediatric Care | Common Childhood Illnesses, Non-emergent Care | N/A | Completed | 2,000 | Open-label | — |
| NCT01583400 Enhanced Collaborative Depression Treatment in Primary Care: The RESPECT-D-E Trial | Depressive Disorder, Major, Depressive Disorder, Minor | N/A | Completed | 131 | RCT, Single-blind | — |
| NCT02365298 Clinical and Laboratory Study of Lysozyme Deposition on Daily Disposable Contact Lenses | Visual Acuity | N/A | Completed | 28 | RCT, Double-blind | — |
| NCT05991960 Evaluation of Real-World Data on the Performance of the TECNIS Odyssey™ IOL | Cataracts | Completed | 96 | — | — | |
| NCT01787760 Controlling Myopia Progression With Soft Contact Lenses | Myopia | N/A | Completed | 221 | RCT, Single-blind | — |
| NCT01825915 Feasibility of a Trial of Laparoscopic Hysterectomy Versus Laparoscopic Sub-Total Hysterectomy | Benign Disease of the Uterus | N/A | Unknown | 50 | RCT, Double-blind | — |
| NCT00834691 An Evaluation of the Causes of Anemia in Patients With Heart Failure | Anemia, Heart Failure | Completed | 180 | — | — | |
| NCT00353613 Prevention of Surgical Site Infections | Surgical Wound Infection | N/A | Completed | 900 | Open-label | — |
| NCT00724945 Comparison of Two Soft Bifocal Contact Lenses | Presbyopia | N/A | Completed | 113 | RCT, Single-blind | — |
| NCT01431469 Efficacy and Tolerance of a Follow-On Formula Fed to Children From 12-48 Months of Age in Salvador, Bahia, Brazil | Acute Respiratory Infection, Diarrheal Disease | N/A | Completed | 250 | RCT, Double-blind | — |
| NCT00366873 Evaluation of Mineral Absorption in Infants Fed Infant Formula | Healthy | N/A | Completed | 44 | RCT, Double-blind | — |
| NCT01650337 mFit: The Mobile Fitness Project | Overweight, Obese | N/A | Completed | 212 | RCT, Single-blind | — |
| NCT06798441 Determination of the Oral Irritation Potential of a Fluoride Rinse in Children | Healthy | N/A | Completed | 161 | RCT, Single-blind | — |
| NCT03516019 eFHS Messaging Trial | Cardiovascular Diseases | N/A | Completed | 650 | RCT, Single-blind | — |
| NCT00940511 Effects of Coordinated Care for Disabled Medicaid Recipients | Chronic Conditions Faced by Medicaid Recipients With Disabilities | N/A | Completed | 2,618 | RCT, Open-label | — |
| NCT01094743 Dispensing Evaluation of a Prototype Contact Lens and a Marketed Contact Lens | Myopia | N/A | Completed | 52 | RCT, Double-blind | — |
| NCT04171518 A Real-World Evidence Study in China of the Catalys Precision Laser System | Cataract | Completed | 139 | — | — | |
| NCT01156376 Oral Irritation Study of Two Experimental Mouthrinses | Oral Manifestations | N/A | Completed | 80 | RCT, Single-blind | — |
| NCT03896100 Assessment of Intracellular Cytokines and Markers in Cells (Phase 3) | Impression Cytology | Completed | 12 | — | — | |
| NCT05123911 A Study of 3 Investigational Products on the Microbiome and Scalp Attributes in Children With Curly Hair | Healthy | N/A | Completed | 35 | Open-label | — |
| NCT00531375 The Effect of Silicone Hydrogel Contact Lenses on Conjunctival Flora | Myopia | N/A | Completed | 60 | RCT, Double-blind | — |
| NCT00508014 Assessing the Effectiveness of Concurrent Peer Review for Patients With Cardiovascular Disease and Diabetes | Cardiovascular Diseases | N/A | Completed | 727 | RCT, Open-label | — |
| NCT01528319 Open-Label Study for Shoulder Dislocation Using MG-1 | Shoulder Dislocation | N/A | Completed | 24 | Open-label | — |
| NCT02515994 Evaluation of a Johnson & Johnson Vision Care Investigational Contact Lens Compared to a Marketed Monthly Replacement Contact Lens | Refractive Error | N/A | Completed | 224 | RCT, Double-blind | — |
| NCT06778057 Clinical Performance of Three Daily Disposable Silicone Hydrogel Contact Lenses | Visual Acuity | N/A | Completed | 22 | RCT, Single-blind | — |
| NCT05393154 Pilot Study of Biopsy Scanner for Evaluation of Bronchoscopic Small Biopsy Specimens to Determine Adequacy | Lung Cancer | Unknown | 70 | — | — | |
| NCT03431441 Clinical Evaluation of 2-Week Reusable ACUVUE 2 Vivid Style | Visual Acuity | N/A | Completed | 26 | Open-label | — |
| NCT01936194 The Effects of Polyunsaturated Fatty Acids (PUFA) on Allergic/Atopic Dermatitis | Atopic Dermatitis | N/A | Withdrawn | — | RCT, Double-blind | — |
| NCT03635320 The CHINA TFNA Study | Femur Fractures | N/A | Completed | 188 | RCT, Single-blind | — |
| NCT00655720 The Effects on Growth of a Non-Routine Infant Formula | Growth | N/A | Completed | 293 | RCT, Double-blind | — |
| NCT03673059 Clinical Trial to Assess the Effects of Topical Lotions on Changes in the Skin Microbiome and Associations With Itch | Microbiota | N/A | Completed | 91 | RCT, Double-blind | OTC Eczema Moisturizer Regimen |
| NCT01234896 Single-dose Nicotine Pharmacokinetics With Four Oral Nicotine Replacement Products | Tobacco Dependence | N/A | Completed | 44 | RCT, Double-blind | Nicotine Medicated Gum, 4 mg Nicotine Gum, 2 mg Nicotine Gum, 4 mg Nicotine Lozenge |
| NCT06654102 A Study to Evaluate the Cutaneous Effects of Deep Ultraviolet A +/- High-Energy Visible Blue Light Exposure | Skin Pigmentation, Photobiology | N/A | Completed | 18 | Open-label | — |
| NCT01626729 Facts-Up-Front Versus Traffic-Light Food Labels | Food Labeling | N/A | Completed | 703 | RCT, Open-label | — |
| NCT01180998 Clinical Evaluation of Two Toric Contact Lenses in Current Non-toric Lens Users | Astigmatism | N/A | Completed | 200 | RCT, Open-label | — |
| NCT00163228 Functional Evaluation of the Total Knee Prostheses:Rising From a Chair | Osteoarthritis, Knee, Osteoarthritis, Hip | Withdrawn | 100 | — | — | |
| NCT01271036 Safety Study of a Sensitive Sensual Touch and Personal Lubricant | Inadequate Lubrication | N/A | Completed | 124 | Open-label | — |
| NCT01093625 Assessment of Daily Disposable Silicone Hydrogel Lens Wear | Myopia | N/A | Completed | 157 | RCT, Single-blind | — |
| NCT01323491 "EASY EFFECTIVE SMOKELESS" With NICORETTE® | Stereotyped Behavior, Tobacco Smoking Behavior | Completed | 184 | — | Nicotine replacement therapy | |
| NCT01552876 Comparative Clinical Evaluation of Soft Toric Lens Designs | Astigmatism, Myopia | N/A | Completed | 42 | RCT, Single-blind | — |
| NCT04529109 Clinical Evaluation of Daily Disposable Etafilcon A Cosmetic Contact Lenses | Visual Acuity | N/A | Completed | 58 | RCT, Double-blind | — |
| NCT00130416 Improving Chronic Disease Care With PatientSite | Depression, Pain | N/A | Completed | 750 | RCT, Single-blind | — |
| NCT04381481 Studying the Impact of Product Packaging in a Virtual Store Environment | Obesity, Childhood | N/A | Completed | 2,374 | RCT, Single-blind | — |
| NCT00220207 Determining the Effect on Patients of Internet-Based Diabetes Disease Management | Diabetes Mellitus, Type 2 | N/A | Completed | 63 | RCT, Open-label | — |
| NCT00241280 Study Intended to Evaluate the Safety and Effectiveness of a Johnson & Johnson Vision Care Inc, (JJVCI) Contact Lens for Use on an Extended-wear Basis for up to 7 Days (6 Nights). | Myopia | N/A | Completed | 504 | RCT, Double-blind | — |
| NCT00641459 A Study on Behavioral and Psychological Symptoms of Dementia | Dementia | Completed | 359 | — | — | |
| NCT06377488 Evaluation of the Clinical Performance of Daily Disposable Silicone Hydrogel Multifocal Toric Contact Lenses | Visual Acuity | N/A | Completed | 176 | Open-label | — |
| NCT04462185 A Prospective Cohort Study of Chinese Patients With Pulmonary Nodules: Prediction of Lung Cancer Using Noninvasive Biomarkers | Pulmonary Nodules | Unknown | 3,000 | — | — | |
| NCT00684125 Evaluation of Different Strategies of Pericardial Drainage After Aortic Valvular Surgery | Pericardial Effusion, Late Cardiac Tamponade | N/A | Completed | 150 | RCT, Open-label | — |
| NCT03913377 Ocular Characteristics in Contact Lens and Spectacle Wear | Visual Acuity | N/A | Completed | 78 | RCT, Open-label | — |
| NCT02960386 An Engagement Engine for Fitness Trackers | Overweight, Obese | N/A | Completed | 184 | Open-label | — |
| NCT01990664 Clinical Evaluation of Lapsed Contact Lens Wearers Who Are Re-fit Into Senofilcon A Contact Lenses | Lapsed Contact Lens Wear | N/A | Completed | 199 | RCT, Open-label | — |
| NCT04441749 nCLE For Diagnosis Of Peripheral Lung Nodules By Robotic Navigational Bronchoscopy | Diagnosis of Peripheral Lung Nodules | Unknown | 25 | — | — | |
| NCT03871543 Late Night Study 2: End-of-Day Assessment of Asymptomatic and Symptomatic Soft Lens Wearers | Visual Acuity | N/A | Completed | 196 | Open-label | — |
| NCT00975585 Clinical Performance Comparison of Two Contact Lenses | Myopia | N/A | Completed | 379 | RCT, Single-blind | — |
| NCT05126407 A Study of Olynth Saline/Ectomed Nasal Drops/Spray Based Upon Previous Usage | Common Cold, Sinusitis | Completed | 87 | — | — | |
| NCT00708032 Clinical Performance of a New Daily Disposable Contact Lens Worn in a Neophyte Population. | Refractive Error, Myopia | N/A | Completed | 74 | RCT, Single-blind | — |
| NCT03408444 Evaluating Soft Contact Lens Prototypes for Myopia Control | Visual Acuity | Completed | 240 | RCT, Double-blind | — | |
| NCT01357434 Comparing Calories at Fast Food Restaurants | Obesity | Completed | 97 | — | — | |
| NCT01936376 A Prospective Observational Study to Evaluate Acute Kidney Injury Biomarkers In Patients Receiving First Cycle of Cisplatin Chemotherapy for Head and Neck Cancers | Head and Neck Cancer | Unknown | 150 | — | — | |
| NCT02481531 Growth and Tolerance of Cow's Milk-Based Infant Formulas | Growth | N/A | Completed | 373 | RCT, Double-blind | — |
| NCT01860378 Vouchers to Promote Tdap Vaccination | Whooping Cough | Early P1 | Completed | 149 | RCT, Double-blind | — |
| NCT06257563 Toolkit for Experiential Well-beiNg in Dementia (TEND) | Dementia, Alzheimer Disease | N/A | Withdrawn | — | Open-label | — |
| NCT05141448 Visual Performance of Soft Contact Lenses With Myopia Control Optics | Visual Acuity | Completed | 79 | RCT, Single-blind | — | |
| NCT02921087 Connecting Contact Lenses and Digital Technology | Asthenopia, Contact Lenses | N/A | Completed | 23 | RCT, Double-blind | — |
| NCT04382599 Designing Impactful Warnings for Sugary Drinks | Health Behavior | N/A | Completed | 1,078 | RCT, Single-blind | — |
| NCT01084707 Multiple-dose Nicotine Pharmacokinetics With a New Oral Nicotine Replacement Product. | Tobacco Dependence | N/A | Completed | 40 | RCT, Open-label | Oral Nicotine, Nicotine Lozenge, Nicotine gum |
| NCT00894140 Study to Assess the Stability, Efficacy and Safety of the Silent™ Hip Prosthesis in Primary Total Hip Replacement | Osteoarthritis | N/A | Completed | 44 | Open-label | — |
| NCT03139578 Short-Term Clinical Comparison of Two Silicone Hydrogel Daily Disposable Contact Lenses | Visual Acuity | N/A | Completed | 51 | RCT, Double-blind | — |
| NCT01361035 Using Effective Provider-Patient Communication to Improve Cancer Screening Among Low Literacy Patients | Cervical Cancer, Breast Cancer | N/A | Completed | 168 | RCT, Single-blind | — |
| NCT01228591 Pilot Dispensing Evaluation of a Plus Power Lens | Hyperopia | N/A | Completed | 38 | RCT, Open-label | — |
| NCT02801396 Clinical Evaluation of Investigational Contact Lenses | Visual Acuity | N/A | Completed | 116 | RCT, Open-label | — |
| NCT01258140 Detection of Pulmonary Embolism With Low-dose CT Pulmonary Angiography | Embolism, Pulmonary | N/A | Completed | 504 | RCT, Single-blind | — |
| NCT05480514 Clinical Evaluation of Daily Disposable Etafilcon A Cosmetic Contact Lenses (2022) | Visual Acuity | N/A | Completed | 89 | RCT, Open-label | — |
| NCT01444313 Prospective Study of the Health Benefits of Ultra-Violet Filtering Contact Lenses | Refractive Errors | N/A | Completed | 40 | RCT, Single-blind | — |
| NCT00672815 The Impact of Texas Senate Bill 42 on Middle School Children's Level of Physical Activity | Obesity, Body Weight | Completed | 141 | — | — | |
| NCT01821508 Clinical Study on Metabolic Surgery Compared to the Best Clinical Treatment in Patients With Type 2 Diabetes Mellitus | Complications of Diabetes Mellitus | N/A | Completed | 100 | RCT, Open-label | — |
| NCT02624791 Evaluating and Improving Functional Driving Vision of Patients With Astigmatism | Astigmatism | N/A | Completed | 11 | RCT, Double-blind | — |
| NCT01084603 Single-dose Nicotine Pharmacokinetics With a New Oral Nicotine Replacement Product | Tobacco Dependence | N/A | Completed | 45 | RCT, Open-label | Oral Nicotine, NiQuitinTM Nicotine Lozenge, Nicorette® Nicotine Gum |
| NCT05045183 A Study to Assess Wound Healing Efficacies of Different Clean, Treat, and Protect Wound Care Regimens Compared to Standard of Care and Untreated | Wound Healing | N/A | Completed | 34 | RCT, Double-blind | Antibiotic Ointment, Antiseptic Wash |
| NCT01055457 Vistakon Investigational Multi-purpose Contact Lens Care Solution. | Contact Lens Wear | N/A | Completed | 315 | RCT, Double-blind | — |
| NCT01152736 Pharmacokinetics With a New Oral Nicotine Replacement Product and Nicorette® Gum | Tobacco Dependence | N/A | Completed | 19 | RCT, Double-blind | Nicotine |
| NCT04116736 ACUVUE® OASYS With Transitions™ Light Intelligent Technology™ Clinical Performance Registry | Vision Satisfaction in Bright Light | Completed | 146 | — | — | |
| NCT04310566 Evaluation of a Daily Disposable Novel Multifocal Contact Lens in a Myopic Population | Visual Acuity | N/A | Completed | 67 | RCT, Single-blind | — |
| NCT04859231 Nutritive Effects of Cow's Milk-Based Formulas Through 18 Months of Age | Nutritive Effects on Brain Myelination | N/A | Terminated | 1 | RCT, Double-blind | — |
| NCT02258477 A Pilot Study: Snacking, Willpower and Glucose Availability | Willpower | N/A | Completed | 37 | RCT, Double-blind | — |
| NCT01454973 Characterization of the Variability of Insulin Secretory Parameters in the Meal Tolerance and the Maximal Stimulation Tests of Healthy Subjects | Type 2 Diabetes | Completed | 25 | — | — | |
| NCT01131403 Clinical Analysis of the Influence of Using the Skin Care Products on the Diaper Area in Comparison with Using a Cotton Wool Cloth, Moistened with Clear Water on the Skin Physiology of the Newborns from the 1st Day to the 4th Week of Life | Postnatal Skin Physiology | Completed | 44 | — | — | |
| NCT06250322 A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens | Cataracts | Completed | 307 | — | — | |
| NCT01731613 Adjustable Fortification of Human Milk Fed to Chinese Preterm Infants | Infant, Premature, Diseases | N/A | Completed | 51 | RCT, Double-blind | — |
| NCT01150604 Depression Management Project | Major Depression, Depression | N/A | Completed | 547 | Open-label | — |
| NCT06965504 INitiation and Titration of Guideline Directed Medical TheRApy in HearT Failure Cardiogenic Shock With ImpElla 5.5 for Cardiac Recovery | Heart Failure, Cardiogenic Shock | N/A | Not Yet Recruiting | 60 | Open-label | — |
| NCT00584220 Evaluation of Two Toric Soft Contact Lenses After Two Weeks of Wear | Astigmatism | N/A | Completed | 96 | RCT, Single-blind | — |
| NCT04977583 Unmet Social Needs Study | Cardiovascular Disease, Hypertension | N/A | Completed | 479 | RCT, Open-label | — |
| NCT04189224 Evaluation of a Reusable Silicone Hydrogel Multifocal Contact Lens | Presbyopia | N/A | Completed | 46 | RCT, Single-blind | — |
| NCT00572962 Prospective Clinical Observational Cohort Study to Evaluate the Use of a Tissue Separating Mesh (Proceed®) in Laparoscopic Ventral Hernia Repair | Ventral Hernia | N/A | Completed | 210 | Open-label | — |
| NCT06591728 PCA Loading Time Before Knee Prosthetic Joint Infection Revision | Prosthesis-Related Infections | N/A | Not Yet Recruiting | 10 | Open-label | — |
| NCT01067963 Self-Management and Resourceful Transition of Type 2 Diabetes With Stage 3 Kidney Disease | Diabetes Mellitus, Type 2, Renal Insufficiency, Chronic | N/A | Terminated | 80 | RCT, Single-blind | — |
| NCT00757133 Prevention of Incisional Hernia by Mesh Augmentation After Midline Laparotomy for Aortic Aneurysm Treatment | Aortic Aneurysm | N/A | Completed | 120 | RCT, Open-label | — |
| NCT02394756 Investigation of Ocular Signs & Symptoms in Wearers Fitted With Contact Lenses Following Digital Device Use | Visual Performance | N/A | Completed | 52 | RCT, Open-label | — |
| NCT02491307 Ginger.io Behavioral Health Study | Anxiety, Depression | N/A | Terminated | 10 | Open-label | — |
| NCT01054807 Non-Dispensing Evaluation of an Investigational Galyfilcon A Soft Contact Lens | Myopia | N/A | Completed | 32 | RCT, Double-blind | — |
| NCT00137722 Outcomes From an Asthma Disease Management Program | Asthma | Completed | — | — | — | |
| NCT01431482 Evaluation of the Composition of Human Milk and Health Outcomes in Children | Respiratory Symptoms, Signs and Symptoms, Digestive | Completed | 245 | — | — | |
| NCT00899041 Functional Evaluation of a Standard and a High-flexion Knee Prosthesis Using Thigh-calf Contact Force Measurements | Arthroplasty, Replacement, Knee | N/A | Completed | 67 | RCT, Double-blind | — |
| NCT01244529 Comparison of Lens Fit and Lens Power of a New Contact Lens to Two Marketed Contact Lenses in a Population of Soft Contact Lens Wearers | Myopia | N/A | Completed | 41 | RCT, Double-blind | — |
| NCT01419626 A Study to Determine the Effects of Adding an Experimental Device With Mouthrinse to Oral Care Regimen | Gingivitis | N/A | Completed | 140 | RCT, Single-blind | — |
| NCT01177917 Evaluation of Mineral Absorption in Infants Fed Infant Formula | Mineral Absorption in the Urine | N/A | Completed | — | — | — |
| NCT01323023 A Study to Examine Health Behavior Change Strategies for Primary Care | Tobacco Use, Risky Drinking | Completed | 4,463 | — | — | |
| NCT04287036 Objective Vision Evaluation of Two Cosmetic Contact Lenses | Visual Acuity | N/A | Completed | 28 | RCT, Single-blind | — |
| NCT04850911 Reward Emotion Learning and Ketamine Study | Depression, Major Depressive Disorder | N/A | Unknown | 70 | RCT, Double-blind | Ketamine Hydrochloride |
| NCT05744193 Feeding Study in VLBW Premature Infants | VLBW - Very Low Birth Weight Infant | N/A | Terminated | 22 | RCT, Double-blind | — |
| NCT03457857 Evaluation of Two Regimens, With Healthy Male and Female Babies, Ages 3-6 Months Old, Using Various Assessments. | Microbiome | N/A | Completed | 38 | RCT, Single-blind | — |
| NCT02611999 Paid Price Information on Image and Procedure Ordering Rates | Healthy | N/A | Completed | 1,205 | RCT, Single-blind | — |
| NCT03103269 Challenge! Adolescent Obesity Prevention | Overweight, Obesity | N/A | Completed | 789 | RCT, Single-blind | — |
| NCT01765972 Open Eye Corneal Swelling With Daily Disposable Contact Lenses and no Lens Wear | Corneal Swelling | N/A | Completed | 39 | RCT, Double-blind | — |
| NCT01239407 Culturally-focused Consultation for Asian Americans and Latino Americans | Depression | N/A | Completed | 122 | RCT, Open-label | — |
| NCT00925457 Evaluating the Risk of Serious Ventricular Arrhythmia and Sudden Cardiac Death Among Users of Domperidone | Arrhythmias, Cardiac | Completed | 1,608 | — | Current Domperidone, Current proton pump inhibitor (PPI) | |
| NCT00211042 A Study of Patients With Pure Red Cell Aplasia Associated With Recombinant Human Erythropoietin Treatment | Pure Red-cell Aplasia | Completed | 52 | — | — | |
| NCT02223754 Evaluation of an Investigational Multifocal Lens | Presbyopia | N/A | Completed | 371 | RCT, Open-label | — |
| NCT03192839 Early DHA Supplementation in Very Low Birth Weight Infants | Prematurity | N/A | Completed | 30 | RCT, Double-blind | — |
| NCT04615507 Evaluation of a Daily Disposable Novel Multifocal Contact Lens in a Myopic Population; Part 2 | Visual Acuity | N/A | Completed | 71 | RCT, Single-blind | — |
| NCT00210639 A Study of Incidence of Musculoskeletal Disorders in Children Who Have Received Levofloxacin or a Standard Non-Fluoroquinolone Therapy for Acute Bacterial Infection | Musculoskeletal Diseases | Completed | 2,233 | — | No intervention | |
| NCT06649019 Evaluation of Lens Rotation in Habitual Wearers of Toric, Soft Contact Lenses | Visual Acuity | N/A | Completed | 6 | RCT, Single-blind | — |
| NCT00727558 A Comparison of Daily Disposable Contact Lenses. | Myopia | N/A | Completed | 248 | RCT, Single-blind | — |
| NCT05258149 Comparison of a Silicone Hydrogel Daily Disposable Multifocal Contact Lens to a Marketed Product | Visual Acuity | N/A | Completed | 143 | RCT, Single-blind | — |
| NCT01791517 Clinical and Laboratory Evaluation of 3 Contact Lenses With 4 Contact Lens Solutions | Contact Lens Solutions | N/A | Completed | 269 | RCT, Double-blind | — |
| NCT01749345 Social Determinants of Health in Diabetes Outcomes | Diabetes Mellitus, Type 2 | Completed | 650 | — | — | |
| NCT04534517 Clinical Evaluation of a Daily Wear Reusable Multifocal Optical Design in a Presbyopic Population | Visual Acuity | N/A | Completed | 119 | Open-label | — |
| NCT02069223 Physiological Impact of Each Component of the Biliopancreatic Diversion With Duodenal Switch and Sleeve Gastrectomy | Biliopancreatic Diversion With Duodenal Switch, Gastrectomy | N/A | Unknown | 45 | RCT, Single-blind | — |
| NCT05876325 Financial and Insurance Assistance- Oncology Financial and Legal Navigation Program | Financial Stress, Pediatric Cancer | N/A | Completed | 61 | Open-label | — |
| NCT04997135 Clinical Evaluation of Therapeutic Meibomian Gland Expression | Visual Acuity, Meibomian Gland | Completed | 16 | — | — | |
| NCT04277455 Effect of Ultrasound Guided Laser Ablation Therapy on Symptomatic Benign Thyroid Nodules | Thyroid Nodule | N/A | Completed | 10 | Open-label | — |
| NCT01181297 Double Blind Controlled Trial of an Extensively Hydrolyzed Formula With a Probiotic vs. an Extensively Hydrolyzed Formula Without a Probiotic | Allergy | N/A | Completed | — | — | — |
| NCT02146235 Music Therapy in the Treatment of Chronic Obstructive Pulmonary Disease | Pulmonary Diseases | N/A | Completed | 68 | RCT, Single-blind | — |
| NCT02173535 Quantitative Study of New Limbal Ring Prototypes | Cosmetic Effect | N/A | Completed | 257 | RCT, Open-label | — |
| NCT01580332 Non-Invasive Biomarkers For Early Detection Of Lung Cancers | Lung Cancer | Completed | 50 | — | — | |
| NCT04923815 A Real-world Study of Cardiac Ablation for PSVT Using ST Catheter | AVRT, AVNRT | Completed | 300 | — | — | |
| NCT04869189 Non-Invasive Assessment of Contact Lens Performance During Use of a Digital Display | Visual Acuity | N/A | Completed | 55 | RCT, Open-label | — |
| NCT05101252 Comparison of a Daily Disposable Multifocal Contact Lens to a Marketed Product | Visual Acuity | N/A | Completed | 77 | RCT, Single-blind | — |
| NCT00593749 Healthy Corner Store Initiative | Obesity Prevention | N/A | Completed | 2,000 | RCT, Open-label | — |
| NCT00916565 Evaluation of Cow Milk-Based Formulas - Functional Proteins | Healthy | Completed | 139 | — | — | |
| NCT01500629 Study of a Topical Nasal Spray to Ease the Symptoms of Hayfever | Rhinitis, Allergic, Seasonal | Early P1 | Completed | 21 | RCT, Double-blind | — |
| NCT02698436 A Study to Evaluate the Effectiveness and Tolerance of Two Acne Treatments on Subjects With Mild to Moderate Acne. | Acne Vulgaris | N/A | Completed | 103 | RCT, Single-blind | 2.5% Benzoyl Peroxide Treatment |
| NCT03733899 An Investigation of the Impact of Localized Topical Anesthesia of the Ocular Surface on End-of-day Contact Lens Discomfort | Visual Acuity | N/A | Completed | 22 | RCT, Single-blind | — |
| NCT06567834 Clinical Evaluation and Comparison of the Tecnis Symfony Optiblue and Tecnis Symfony IOLs | Cataract, Presbyopia | N/A | Completed | 60 | RCT, Double-blind | — |
| NCT00887302 Metabolomics of Roux-en-Y Gastric Bypass (RYGB) With Gastrostomy | Type II Diabetes Mellitus, Obesity | Completed | 13 | — | — | |
| NCT04178772 Characterizing Successful Myopic Multifocal Contact Lens Wearers | Visual Acuity | N/A | Terminated | 29 | Open-label | — |
| NCT03645512 Resilience Intervention for Critical Care Nurses | Stress | N/A | Completed | 108 | RCT, Open-label | — |
| NCT01943591 DELTA Trial: Does Embolization With Larger Coils Lead to Better Treatment of Aneurysms Trial | Cerebral Aneurysm | N/A | Completed | 210 | RCT, Single-blind | — |
| NCT01834924 Improving Communication of Medication Instructions to Parents | Medication Errors, Medication Adherence | N/A | Completed | 1,196 | Single-blind | — |
| NCT00762502 Comparison of Senofilcon A Toric Lenses to Balafilcon A Toric Lenses Over Extended Wear Period | Astigmatism | N/A | Completed | 112 | RCT, Open-label | — |
| NCT03581981 Improving Function Through Primary Care Treatment of Posttraumatic Stress Disorder (PTSD) | Posttraumatic Stress Disorder | N/A | Completed | 120 | RCT, Single-blind | — |
| NCT00304603 Mode of Action of Topiramate in the Treatment of Obese Patients With and Without Type 2 Diabetes Mellitus | Obesity, Diabetes Mellitus Type 2 | Completed | 1,145 | — | — | |
| NCT01152749 Bioequivalence Between an Oral Nicotine Replacement Product and Nicorette® Gum | Tobacco Dependence | N/A | Completed | 76 | RCT, Double-blind | Nicotine, Nicotine Gum |
| NCT07228312 A Study of Choydar Flow-Directed Mesh Stent in the Treatment of Unruptured Intracranial Aneurysms | Intracranial Aneurysm | Not Yet Recruiting | 200 | — | — | |
| NCT02988375 Sleep to Prevent Evolving Affecting Disorders | Insomnia, Primary, Depression | N/A | Completed | 1,385 | RCT, Open-label | — |
| NCT03142984 UK Baby Study Using a Baby Wash and Lotion Regimen | Newborns | N/A | Terminated | 82 | RCT, Double-blind | — |
| NCT01558752 A Clinical Trial of a Metal on Poly Component Versus CORAIL Stem: A Bone Mineral Density Study | Total Hip Arthroplasty | N/A | Completed | 88 | RCT, Single-blind | — |
| NCT02399046 A Clinical Trial Study of Knee System in Primary Total Knee Arthroplasty in China | Arthritis, Rheumatoid, Osteoarthritis | N/A | Completed | 160 | RCT, Single-blind | — |
| NCT00232986 A Comparison of Survey Methodologies to Elicit Sensitive Information From Adolescents in Urban India | Unmarried Male and Female Adolescents in the Age Group 15-19 Years in Pre-Identified Slums in Delhi, India | Completed | 960 | — | — | |
| NCT03228212 Evaluation of Approved and Investigational Contact Lenses | Visual Acuity | N/A | Completed | 133 | RCT, Single-blind | — |
| NCT03796052 Study Determining Safety and Efficacy of Avena Sativa (Oat) Skincare Products for Treating Skin Dryness and Itching in Cancer Patients | Ichthyosis, Pruritus | N/A | Completed | 53 | Open-label | — |
| NCT05051358 Therapeutic Endoscopic Ultrasound for Gastrointestinal Disorders: A Multicenter Registry Study | Therapeutic Endoscopic Ultrasound, Advanced Endoscopy | Unknown | 5,000 | — | — | |
| NCT05589038 A Study of a Baby Wash/Shampoo and Baby Lotion Versus Baby Wash/Shampoo Alone for Impact on Skin Barrier and Microbiome on Newborns | Healthy | N/A | Terminated | 53 | RCT, Single-blind | — |
| NCT02310126 Handling Comparison Between Two Contact Lens Types | Presbyopia | N/A | Completed | 195 | RCT, Single-blind | — |
| NCT03476655 Clinical Outcomes of Chronic Lymphocytic Leukemia (CCL) and Mantle Cell Lymphoma (MCL) Participants Treated With Ibrutinib: A Medical Chart Review From India | Leukemia, Lymphocytic, Chronic, B-Cell, Lymphoma, Mantle-Cell | Completed | 40 | — | Ibrutinib | |
| NCT05601544 The Effects of Contact Lenses With UV/HEV-Filter on Visual Function | Visual Acuity | N/A | Completed | 145 | RCT, Double-blind | — |
| NCT01205698 Glycemic Index of Foods | Glycemic Response | N/A | Completed | — | — | — |
| NCT03707821 Design Validation of Senofilcon A With New UV-blocking Additive | Visual Acuity | N/A | Completed | 253 | RCT, Single-blind | — |
| NCT00778934 In-Home Use Study to Evaluate Use of an Intimate Health Product in Females | Coitus | N/A | Completed | 79 | Single-blind | — |
| NCT00195169 Quality of Life After Myocardial Infarction | Myocardial Infarction | Completed | 213 | — | — | |
| NCT04454983 Lipiflow vs iLux Patient Acceptance and Comfort Study | Meibomian Gland Dysfunction, Dry Eye | N/A | Completed | 43 | RCT, Open-label | — |
| NCT01582594 A Registration Study to Evaluate the Performance of CHIRON® RIBA® HCV 3.0 SIA in HCV Antibody Detection | Hepatitis C | Terminated | 795 | — | — | |
| NCT04059666 Gastrointestinal Tract Microbiome in Healthy Term Infants Receiving Mother'S-own Breast Milk or Cow's Milk-based Infant Formulas | Gastrointestinal Microbiome | N/A | Terminated | 57 | RCT, Double-blind | — |
| NCT01440985 A Study on the Effects of Two Nicotine Replacement Products on Tooth Staining | Tobacco Dependence | N/A | Completed | 200 | RCT, Single-blind | Nicotine, Nicotine, Nicotine |
| NCT04235413 Fruits and Vegetables Incentives Study | Obesity, Fruit and Vegetable Intake | N/A | Completed | 244 | RCT, Open-label | — |
| NCT00865774 The Teachable Moment: Screening and Brief Intervention for Admitted Trauma Patients | Alcoholism | N/A | Completed | 333 | RCT, Single-blind | — |
| NCT03771274 Tecnis ZLB00 & Symfony Intraocular Lens Combination Outcomes | Cataract Bilateral, Presbyopia | N/A | Completed | 39 | Open-label | — |
| NCT01244516 Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses | Myopia | N/A | Completed | 540 | RCT, Single-blind | — |
| NCT04096898 Senofilcon A Lenses in Moderate to Severe Dry Eye Disease | Moderate to Severe Dry Eye Disease | N/A | Unknown | 32 | Double-blind | — |
| NCT00214487 Bifocal Soft Contact Lenses and Their Effect on Myopia Progression in Children and Adolescents. | Myopia, Esophoria | N/A | Completed | 78 | RCT, Double-blind | — |
| NCT06243627 A Study to Assess Safety and Improvement in Skin Barrier After Using 2 Facial Sunscreens in Adults With Sensitive Skin | Healthy | N/A | Completed | 35 | RCT, Open-label | — |
| NCT04442477 Neurodevelopment at 5.5 Years of Age in Children Who Received Infant Formula With Enriched Protein Fractions | Cognitive Ability, General | Completed | 116 | — | — | |
| NCT07511166 A Study of Varipulse Catheter in Participants With Paroxysmal Atrial Fibrillation Under Optimized Sedation | Atrial Fibrillation | Not Yet Recruiting | 300 | — | — | |
| NCT03731195 GentleTouch (Study to Evaluate Somatosensory Evoked Potential (SSEP) Responses to Affective Touch and How it Develops in Healthy Term Babies) | Pleasant Touch, Cortical Response | Completed | 90 | — | — | |
| NCT01041014 Cost Effectiveness of Language Services in Hospital Emergency Departments (EDs) | Language Discordance | N/A | Completed | 447 | RCT, Open-label | — |
| NCT00665938 Followup of Infants Fed Non-routine Infant Formula | Healthy | N/A | Completed | 183 | RCT, Double-blind | — |
| NCT02346344 Outpatient Characterization of the Variability of Insulin Secretory Parameters in the Meal Tolerance and the Maximal Stimulation Tests of Subjects With Type 2 Diabetes Mellitus | Type 2 Diabetes | Completed | 20 | — | — | |
| NCT00584831 Effect of Eye Movement on Toric Lens Orientation and Visual Acuity | Astigmatism | N/A | Completed | 40 | RCT, Single-blind | — |
| NCT01579045 Effect of Head and Gaze Position on Soft Toric Contact Lens Performance | Astigmatism, Myopia | N/A | Completed | 24 | RCT, Single-blind | — |
| NCT03319212 Clinical Characterization of Symptomatic Populations | Ametropia | N/A | Completed | 105 | Open-label | — |
| NCT01669629 Comparison of Two Daily Disposable Contact Lenses Over 1-week of Wear | Myopia | N/A | Completed | 183 | RCT, Double-blind | — |
| NCT01482819 Evaluation of Daytime Corneal Swelling During Wear of Galyfilcon A Lenses | Myopia | N/A | Completed | 21 | RCT, Single-blind | — |
| NCT03164330 Illinois Workplace Wellness Study | Employee Health and Well-being | N/A | Unknown | 4,834 | RCT, Single-blind | — |
| NCT03791619 Post-Approval Study of the TECNIS SYMFONY® Toric Lenses | Cataract, Corneal Astigmatism | N/A | Completed | 475 | Open-label | — |
| NCT02328937 Central Corneal Swelling With Silicone Hydrogel Materials | Corneal Swelling | N/A | Completed | 41 | RCT, Open-label | — |
| NCT03168542 Clinical Evaluation of Fitting Investigational Contact Lenses Phase 2 | Visual Acuity | N/A | Completed | 23 | Open-label | — |
| NCT03605303 Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process | Refractive Error Correction | N/A | Terminated | 3 | RCT, Double-blind | — |
| NCT04766879 Spatial Repellents for the Prevention of Malaria in Kenya | Malaria | N/A | Completed | 5,984 | RCT, Double-blind | — |
| NCT03949335 Clinical Investigation of the Safety and Effectiveness of an Investigational Model of the TECNIS® Intraocular Lens | Cataract, Corneal Astigmatism | N/A | Completed | 272 | RCT, Double-blind | — |
| NCT03406520 Chlorhexidine Disk for Prevention of Exit-site Infection in Peritoneal Dialysis Patients | Peritoneal Dialysis Catheter Exit Site Infection | N/A | Completed | 50 | Open-label | — |
| NCT05634408 Evaluating ACUVUE® Abiliti™ 1-Day Soft Therapeutic Lenses for Myopia Management | Visual Acuity | N/A | Completed | 75 | Open-label | — |
| NCT05502289 Clinical Evaluation of Delefilcon A and Verofilcon A Daily Disposable Toric Soft Contact Lenses Over One Week of Wear | Ocular Physiology | N/A | Completed | 66 | RCT, Double-blind | — |
| NCT01055613 Investigational Multi-purpose Contact Lens Care Solution. | Contact Lens Wear | N/A | Completed | 312 | RCT, Double-blind | — |
| NCT05584124 rTMS for Post-stroke Fatigue | Stroke, Stroke, Chronic | N/A | SUSPENDED | 60 | RCT, Single-blind | — |
| NCT05565625 A Study to Evaluate the Whitening Effect of Mineral Sunscreens in Multi-Cultural Skin Tones | Sunscreen | N/A | Completed | 97 | Open-label | — |
| NCT00359996 Improving Diabetes Care Collaboratively in the Community | Diabetes | N/A | Completed | 6,993 | RCT, Open-label | — |
| NCT04040933 A Study to Assess Wound Healing Efficacies of Different Adhesive Bandages | Wound Healing | N/A | Completed | 36 | RCT, Single-blind | — |
| NCT06542276 Single Lipiflow Treatment to Reduce Pharmacologic Burden in DED | MGD-Meibomian Gland Dysfunction | N/A | By Invite | 30 | Open-label | — |
| NCT01228617 Single-dose Pharmacokinetics of Oral Nicotine Replacement Products | Tobacco Dependence | N/A | Completed | 40 | RCT, Double-blind | Nicotine, Nicotine Gum |
| NCT02493218 D-Stress Baltimore: School-based Mindfulness Instruction | Coping, Stress Disorders, Post-Traumatic | N/A | Completed | 400 | RCT, Double-blind | — |
| NCT00531518 Early Detection and Intervention for the Prevention of Psychosis | Schizophrenia, Bipolar Disorder | N/A | Completed | 292 | Single-blind | aripiprazole; fluoxetine; bupropion; sertraline; lamotrigine |
| NCT03436082 Post-Market Surveillance With a Novel mHealth Platform | Gastrectomy, Atrial Fibrillation | Completed | 60 | — | — | |
| NCT06209476 Clinical Investigation on Assessing the Repeatability and Reproducibility of Central and Peripheral Refractive Error | Refractive Error | Completed | 30 | — | — | |
| NCT02595502 Clinical Evaluation of Two Silicone Hydrogel Daily Disposable Contact Lenses | Vision Disorders | N/A | Completed | 286 | RCT, Single-blind | — |
| NCT02394925 Acceptance & Tolerance Study of Multifocal Contact Lenses by Functional Emmetropes | Vision Correction | N/A | Completed | 113 | Open-label | — |
| NCT01279265 Effect of Lactobacillus Rhamnosus GG (LGG) on Infant Colic | Colic, Inflammation | N/A | Completed | 30 | RCT, Double-blind | — |
| NCT03600389 Patient Priorities Care (PPC) | Multiple Chronic Conditions | N/A | Completed | 414 | Single-blind | — |
| NCT00712608 The Evaluation of Cow's Milk Formula - Study B | Healthy Term Infants | N/A | Completed | 399 | RCT, Double-blind | — |
| NCT01180985 Dispensing Evaluation of a Galyfilcon A Prototype Lens and a Marketed Contact Lens | Myopia | N/A | Completed | 53 | RCT, Open-label | — |
| NCT05555199 Injection of 99mTc-nanocolloid and ICG to Identify, Retrieve and Qualify TDLN in Early-stage NSCLC | Early-stage Lung Cancer | N/A | Completed | 72 | Open-label | ICG |
| NCT02952235 Evaluation of Sunscreens Under Actual Use Conditions | Sun Protection | N/A | Completed | 199 | RCT, Double-blind | — |
| NCT00511784 Relative Risks for Non-fatal Venous Thromboembolism, Ischemic Stroke and Myocardial Infarction in Users of ORTHO EVRA(Norelgestromin and Ethinyl Estradiol Contraceptive Patch) Compared to Levonorgestrel-containing Oral Contraceptives. | Contraception, Female Contraception | Completed | 440 | — | — | |
| NCT05047978 Growth and Tolerance of a Partially Hydrolyzed Infant Formula | Growth | N/A | Completed | 244 | RCT, Double-blind | — |
| NCT02450747 Performance of a Multifocal Contact Lens - Presbyopia Study | Presbyopia | N/A | Completed | 44 | Open-label | — |
| NCT05554640 Clinical Performance of Two Daily Disposable Silicone Hydrogel Contact Lenses | Visual Acuity | N/A | Completed | 16 | RCT, Single-blind | — |
| NCT02386540 Health Coach Program to Improve Chronic Disease Outcomes Following an Emergency Department Visit | Diabetes Mellitus, Hypertension | N/A | Completed | 295 | RCT, Single-blind | — |
| NCT06616558 A Study to Assess the Effectiveness of Sunscreen on Oil Control, Moisturization, and Skin Barrier Integrity in Adults With Oily Skin | Oily Skin | N/A | Completed | 32 | RCT, Open-label | — |
| NCT00891774 Post Market Safety Study and Effectiveness With Evolence in Subjects With Skin Color Types IV-VI | Non Therapeutic Body Modification | N/A | Completed | 172 | Open-label | — |
| NCT04811690 Front-of-package Marketing on Fruit Drinks: Online RCT | Consumer Behavior, Consumer Preference | N/A | Completed | 5,028 | RCT, Single-blind | — |
| NCT01829191 Controlling Myopia Progression With Soft Contact Lenses (Contact Lens Control) | Myopia | N/A | Completed | 174 | RCT, Double-blind | — |
| NCT04669080 Asthma Clinics Helping Expand Cost Conversations | Asthma in Children | N/A | Completed | 65 | Open-label | — |
| NCT01009554 Oral Tissue Tolerance of a Mouthrinse | Dental Health | N/A | Completed | 96 | RCT, Single-blind | Sodium Fluoride Dentifrice |
| NCT01016652 Clinical Evaluation of a Multifocal Contact Lens on Symptomatic Patients | Presbyopia | N/A | Completed | 49 | RCT, Double-blind | — |
| NCT01079884 Gastroesophageal Reflux Disease (GERD)/Nighttime Heartburn and Driving Performance | GERD | N/A | Completed | 18 | RCT, Open-label | esomeprazole 40 mg |
| NCT01829230 Myopia Progression After Ceasing Myopia Control Contact Lens Wear | Myopia | N/A | Completed | 82 | Open-label | — |
| NCT04073186 Evaluation of A Marketed Silicone Hydrogel Spherical Lens Used for Monovision Correction of Presbyopia | Visual Acuity | N/A | Completed | 91 | Open-label | — |