6,678 trials
Papulopustular Rosacea
Primary: Rosacea Score on the Visual Analog Scale — 4.50; 4.52; 3.77; 3.06 units on a scale
Psoriasis
Primary: Improvement in Quality of Life Measured by Change in Psychological General Well-Being Scale (PGWB) at Week 36 From Baseline. — 23.97 units on a scale
Epilepsy
Primary: Percentage of Subjects Continuing the Allocated Investigational Treatment From the First Study Treatment Intake to Week 52, After the Beginning of Investigational…
Obesity
Primary: Change in iGFR (Glomerular Filtration Rate as Measured by Iohexol Clearance) From Baseline to End of Treatment — -14.92; 1.08 mL/min/1.73 m^2
Chronic Myelogenous Leukemia in Chronic Phase
Primary: Number of Participants With Confirmed Complete Molecular Response (CMR) — 34 Participants
Wound Infection
Primary: Number of Operating Room Visits — 2.5; 2.8 Operative Room Visits
HIV
Primary: Efficacy as Assessed by the Number of Participants Who Were HIV Positive at 6 Months — 0 participants
Autism · Pervasive Development Disorder · Asperger's Disorder
Primary: Percentage of Participants Who Were Attention Deficit Hyperactivity Disorder (ADHD) Respondents — 45.2; 46.9; 29.0; 19.4 percentage of participants — p=0.47
Infertility, Female
Primary: Number of Retrieved Oocytes — 13.14; 10.29 Oocytes
Diabetes Mellitus, Non-Insulin-Dependent
Primary: Absolute Change From Baseline in Haemoglobin A1c (HbA1c) — -1.19; -1.59; -1.61 (%)
Anorexia Nervosa
Primary: Change in Eating Disorder Inventory-2 Drive for Thinness Subscale (DT) — 1.36; 3.93 units on a scale
Acute Heart Failure
Primary: Evaluation of Mean Urine Output Volume During the Infusion Period — 2505; 2140 mL — p=0.04
Infections
Primary: Clinical Response at Study Day 4 in the Modified Intent-to-Treat (MITT) Population — 14; 8; 16; 8 participants
Epilepsy
Primary: Percentage of Participants Who Achieved Reduction in Daily VPA Dose — 60.6 Percentage of participants
Non-Squamous Non-Small Cell Lung Cancer
Primary: Progression-Free Survival (PFS) — 12.846 Months