12,372 trials
Heroin Addiction
Primary: Treatment Retention in the Community — 23.1; 91.3; 166.0 Days in community treatment
Varicose Veins
Primary: Change in Patient-Reported Symptoms of Varicose Veins (VVSymQ Score) — -2.00; -5.34; -6.01; -5.06 units on a scale — p=<0.0001
Cushing's Syndrome
Primary: Number of Participants With Adverse Events — 30 participants
Hepatitis C
Primary: Percentage of Participants With Sustained Virologic Response 12 Weeks After Stopping All Study Drugs (SVR12) — 67; 67 percentage of participants
Diphtheria · Tetanus · Pertussis
Primary: Number of Participants Achieving Seroprotection for Anti Hep-B After a Primary Series of Vaccination With Either DTaP-IPV-Hep B-PRP~T or Infanrix Hexa™ — 131; 130…
Vestibulodynia · Vulvodynia
Primary: Pain Rating Index — 12.3 units on a scale — p=.001
Advanced Non-Small Cell Lung Cancer
Primary: Progression Free Survival Without Grade 4 Toxicity (G4PFS) as Measured by the Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0 — 3.91; 2.86 months…
Major Depressive Disorder
Primary: Number of Patients With Adverse Events (AEs) — 391; 18; 42 participants
Lymphocytic Leukemia, Chronic
Primary: Progression-free Survival (PFS) — 31.1; 11.1 Months — p=<0.0001
Hepatitis B · Polio · Diphtheria
Primary: Number of Participants Achieving Seroprotection Against Hepatitis B and Haemophilus Influenzae Type b Post-vaccination With Either DTaP-IPV-Hep B-PRP~T + Prevnar™ or…
Treatment Resistant Depression
Primary: Time to Relapse by Any Criteria — NA; NA days — p=<0.001
Myopia, Pathological
Primary: Mean Change in Best Corrected Visual Acuity (BCVA) as Measured by Early Treatment Diabetic Retinopathy Study (ETDRS) From Baseline to Week 24 - Last Observation Carried…
Asthma
Primary: Mean Change From Baseline (BL) in Daily Evening (PM) Peak Expiratory Flow (PEF) Averaged Over the 12-week Treatment Period — -11.8; 39.2 Liters/minute (L/min) — p=<0.001
Chronic Otitis Media
Primary: FLACC Behavioral Pain Assessment Scale Scores — 5; 3; 1; 2 units on a scale
Bipolar Depression
Primary: Number of Participants With Serious and Non-serious Treatment-emergent Adverse Events Who Have Completed 24 Weeks of Extension Study Treatment — 529 participants