65,437 trials
Myopia
Primary: Slit Lamp Findings — 7; 2 Number of Subject Eyes
Type 1 Diabetes Mellitus
Primary: Change From Baseline in Glucagon-Stimulated C-Peptide AUC at 24 Months — -5.20; -4.83 nmol*min/L — p=0.33
Osteoporosis, Postmenopausal
Primary: Number of Participants Receiving All Prescriptions and Injections of Denosumab From the Initial Prescribing Physician's Office — 295; 296 participants
Procedural Sedation
Primary: Level of Sedation Throughout the Entire Procedure — 22; 9; 10; 1 participants
Infection and Inflammatory Reaction
Primary: Number of Participants With Chromium and Cobalt Ion Levels Above 7ug/l — 14; 0 participants above limit
Advanced Breast Cancer
Primary: Number of Participants With Disease Progression (PD) or Death — 35; 40 participants
Primary Disease
Primary: Average Adjusted Symptom Score (AAdSS) — 5.58; 6.07 Units on a scale (range: 0 to 18) — p=0.2344
Lung Cancer
Primary: Incidence of Chronic Neurotoxicity — 60; 85; 89 percentage of participants
Advanced Solid Malignancy, · Safety and Tolerability, · Pharmacokinetics, Pharmacodynamics,
Primary: Ratio of Css,Max for Day 4 to Day 11 — 1.02; 0.67 Ratio
Liposarcoma · Surgically Unresectable Liposarcoma · Metastatic Liposarcoma
Primary: 12-week Progression Free Rate — 68.29 percentage of participants
Chemotherapy-Induced Nausea and Vomiting
Primary: Percentage of Participants With Complete Response of Acute and Delayed Chemotherapy Induced Nausea and Vomiting — 29.6; 46.3; 24.1 percentage of participants
Refractory Multiple Myeloma
Primary: Dose-limiting Toxicity (DLT) (Phase I) — 0; 0; 0; 0 participants
Allergy
Primary: Average Adjusted Symptom Score (AAdSS) — 3.39; 3.25; 5.21 Units on a scale (range: 0 to 18) — p=< 0.0001
Osteoarthritis
Primary: Number of Participants Demonstrating Proper Use of Arcoxia® and Celebrex® — 65; 118 Participants
Anemia
Primary: Median Time to First Cardiovascular Event — NA; NA days — p=0.2036