65,437 trials
Barrett's Esophagus
Primary: Number of Participants With Tolerability of the Procedure — 6 Participants
Polymorphism-Genetic · Pain · Addiction
Primary: 11C Raclopride Binding Potential in Caudate — 3.25; 3.45 mCi/ml
Postherpetic Neuralgia
Primary: Change From Baseline to Week 4 in the Weekly Average of the Daily Average Numeric Rating Scale (NRS) Pain Scores Using a Mixed Model for Repeated Measures — 5.37; 5.60…
Hepatitis C, Chronic
Primary: Percentage of Participants With Partial Early Virological Response (pEVR) to Study Treatment — 15.7 Percentage of participants
Asthma
Primary: Annualized Rate of Severe Exacerbation Events During The 52-Week Treatment Period: Intent-to-Treat (ITT) Population — 0.871; 0.456; 0.970; 0.524 Exacerbation per…
Asthma
Primary: Percentage Reduction From Baseline in Oral Corticosteroids (OCS) Dose at Week 24 While Maintaining Asthma Control — 41.85; 70.09 Percentage reduction from baseline — p=<…
HIV-1
Primary: Percentage of Participants Achieving Plasma HIV-1 RNA <50 Copies/mL at Week 48 — 83.8; 79.9 Percentage of participants
Attention Deficit Hyperactivity Disorder (ADHD) · Deficient Emotional Self-Regulation (DESR)
Primary: Mean Change From Baseline to Endpoint on the BRIEF-A Emotional Control Scale — -7; -33 T-Score
Cervical Radiculopathy
Primary: Upper Limb Neurodynamic Tesnion (UNLT) Range of Motion — 4.60; 16.00 degrees
Rett Syndrome
Primary: Change in Mullen; Visual Reception Sub-scale Scores, Pre- and Post-Intervention — 5.45; 6.61; 6.64; 6.57 score on a scale — p=.211
Depressive Disorder, Major
Primary: Pharmacokinetics: Maximum Plasma Concentration (Cmax) of Ethinyl Estradiol and Norelgestromin — 79.0; 80.9; 1438; 1574 picograms/milliliter (pg/mL)
Major Depressive Disorder
Primary: Maximum, Minimum and Average Changes in Heart Rate — 33.4; 15.7; 35.7; 31.1 beats per minute (bpm)
Stress Urinary Incontinence
Primary: Change in 1-hour Pad Weight Test From Baseline to 24 Month Follow-up — 48.7; 6.6 grams
Advanced Solid Tumors
Primary: Number of Participants With Adverse Events (AEs) or Deaths — 2; 3; 2; 0 Participants
Carpal Tunnel Syndrome
Primary: Number of Patients Who Have Had Carpal Tunnel Release Surgery on the Study Hand — 31; 34; 36 Participants