65,437 trials
Refractory Ventricular Tachycardia
Primary: ICD (Implantable Cardioverter Defibrillator) Shock Free Survival — 1 Participants
Small Fiber Neuropathy
Primary: Change in Weekly Average of Daily Pain Intensity on the 11 Point NRS — -2.018; -0.933 units on a scale — p=<0.0001
Depression, Anxiety · Suicidal Ideation · Stress
Primary: Change in Salivary Cortisol Levels — -0.26; -0.17 ug/dl
Infraorbital Hollowing
Primary: Percentage of Participants With at Least a 1-point Improvement Change From Baseline on the Allergan Infraorbital Hollows Scale (AIHS) Based on Evaluating Investigator's…
Benign Prostatic Hyperplasia
Primary: Number of Adverse Events Reported — 7 adverse events
Spinal Cord Injuries · Neuropathic Pain
Primary: Neuropathic Pain — 13.3; 15.6 units on a scale — p=0.67
Cytomegalovirus Infections
Primary: Percentage of Participants With a Solicited Injection-site Adverse Event (AE) — 100.0; 83.3; 0.0; 33.3 Percentage of participants
Nicotine Dependence · Tobacco Smoking
Primary: Smoking Lapse Analogue Task (Delay Score) — 11.5; 10.9 minutes
Allergic Bronchopulmonary Aspergillosis
Primary: Number of Participants With Treatment-Emergent Adverse Events (TEAE) — 0; 3; 2; 2 participants
Solid Neoplasms
Primary: Number of Participants Experiencing Dose-limiting Toxicities (DLTs) as Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0 by the…
Healthy Volunteers · Alzheimer Disease · Molecular Imaging
Primary: Determination of the Regional Density and Distribution of I2BS in Healthy Human Brain (1TCM Model) — 44.5; 39.3; 62.7; 38.6 mL/cm^3
Acute Coronary Syndrome (ACS)
Primary: Mean Change From Baseline to Week 4 in P2Y12 Reaction Units During Period 1 — -18.2 P2Y12 reaction unit
Migraine
Primary: Frequency of Moderate to Severe Headache Days — 9.3; 9.1 days
Prostate Cancer
Primary: Safety Assessed by Development of Adverse Events and Dose-limiting Toxicity to Determine Maximum Tolerated Dose — 3; 3; 6; 0 Participants
Non-alcoholic Steatohepatitis (NASH)
Primary: Number of Participants With Adverse Events — 42; 41; 40; 42 Participants