65,437 trials
Upper Back Pain
Primary: Mean Change From Baseline of Both AM and PM Spasm Assessment Scores — 1.66; 1.87; 1.91; 1.54 Score on a Scale — p=0.68
Influenza
Primary: Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against 2 Strains of Influenza Disease — NA; NA; NA; NA Titer
Liver Neoplasms · Adenoma · Carcinoma
Primary: Percentage of Participants With Overall Change in Additional Diagnostic Information Obtained When Comparing the Combined Precontrast/Postcontrast Images With the…
Genotype 1 Chronic Hepatitis C
Primary: EVR (Early Virologic Response) — 79.4; 78.5 percentage of participants — p=1.000
Non-small Cell Lung Cancer
Primary: Disease Free Survival (DFS) — 50.5; 48.2 months — p=0.3235
Diabetes Mellitus, Type 2
Primary: Change From Baseline in Glycosylated Hemoglobin A1c (HbA1c) After 14 Weeks Treatment — -0.99; -0.98 percent — p=<0.0001
Schizophrenia
Primary: Change From Baseline in Positive and Negative Syndrome Scale (PANSS) Total Score at Week 48 — 11.57; 6.43; 16.36 Units on a scale
Major Depressive Disorder
Primary: Change in Depression Severity as Measured by the 9-item Patient Health Questionnaire (PHQ-9) — 14.6; 6.1; 8.5 units on a scale — p=0.000
Lymphoma · Myeloma · Leukemia
Primary: Toxicity — 5; 3; 10; 17 participants
Melanoma (Skin)
Primary: Plasma b-FGF Level Response — 34.5 percentage of participants — p=<0.001
Atrial Fibrillation
Primary: Proportion of Subjects Who Were Free From Atrial Arrhythmia at One Year. — 10; 18; 29; 20 participants — p=0.048
Atrial Fibrillation · Tachycardia, Supraventricular
Primary: Number of Subjects With Operative and Post-operative Serious Adverse Events — 4; 1 participants
Advanced Parkinson's Disease
Primary: Clinical Global Impression (CGI) Item 4 (Side Effects) at the End of the Treatment Period — 61; 22; 3; 3 participants
Body Contouring
Primary: Combined Circumference in Inches of the Waist, Hips and Bilateral Thighs — -3.895; -1.136 inches
Non-Small Cell Lung Carcinoma · Breast Cancer · Melanoma
Primary: Number of Participants With Dose-Limiting Toxicity (DLT) — 0; 0; 0; 0 Participants