65,437 trials
HIV Lipodystrophy
Primary: Insulin Resistance (HOMA Index) — 1.6; 1.8 units on a scale
Chronic Obstructive Pulmonary Disease
Primary: Change From Baseline in 1-hour Morning Post-dose Forced Expiratory Volume in One Second (FEV1) — 0.247; 0.226; 0.139; 0.165 Liters — p=<0.0001
Cervical Cancer · Oropharyngeal Cancer · Vaginal Cancer
Primary: Number of Participants With an Objective Clinical Response — 3; 2; 2; 0 Participants
Eosinophilic Esophagitis
Primary: Number of Participants With Treatment-emergent Adverse Events (AEs), Serious AEs, or Discontinuation Due to AEs — 177; 38; 63; 0 participants
Actinic Keratosis
Primary: Percentage of Participants With Complete Response 12 Weeks After the Last Photodynamic Therapy (PDT), ITT — 17.1; 78.2; 64.2 percentage of patients — p=0.0000
Non-Small Cell Lung Cancer
Primary: Percentage of Participants Achieving Objective Response (ORR) Per Response Evaluation Criteria In Solid Tumors (RECIST) Version (v) 1.1 as Assessed by Independent Review…
Multiple Sclerosis, Relapsing Forms of Multiple Sclerosis
Primary: Change From Baseline (BL) in Expanded Disability Status Scale (EDSS) — 0.58; 1.17 score on a scale — p=0.0155
Very Long-chain acylCoA Dehydrogenase (VLCAD) Deficiency · Carnitine Palmitoyltransferase 2 (CPT2) Deficiency · Mitochondrial Trifunctional Protein (TFP) Deficiency
Primary: Energy Expenditure — -73; 107 kcal/day
Type 2 Diabetes
Primary: Number of Children With Documented Risk Factors for Type 2 Diabetes — 283; 282 Participants
Physician Behavior
Primary: The Number of Prompts That Were Responded to — 672; 712 Participants
Asthma
Primary: Number of Participants With Sufficient Vitamin D Levels (≥30 ng/ml) After 8 Weeks of Supplementation — 8; 6; 4 participants
Delayed Alcohol Induced Headache
Primary: Headache Severity 2 Hours Post Treatment — 2.18; 2.09; 0.85; 1.17 units on a scale
Dentin Sensitivity
Primary: Change From Baseline in Schiff Sensitivity Score on Day 3 — -0.96; -0.77 Score on a scale — p=0.1575
Critical Illness
Primary: Central Line Placement Success — 82; 108 participants — p=<0.001
Churg Strauss Syndrome
Primary: Number of Participants With Indicated Side Effects — 3; 1; 0; 1 Participants