65,437 trials
Cervical Intraepithelial Neoplasia
Primary: Screening Uptake — 2519; 0; 2618; 599 participants
Rheumatoid Arthritis
Primary: Absolute C-reactive Protein (CRP) Values at Day 98 - As Treated Population — 12.85; 14.25; 21.85; 16.60 mg/L
Skin Diseases, Infectious
Primary: Skin Abscess Resolution — 4; 3 participants
Macular Edema · Retinal Vein Occlusion
Primary: Change From Baseline at Month 1 in Retinal Thickness in the Study Eye During Stage 1 — 500.2; 495.8; 499.5; 468.3 Microns
Conjunctivitis, Allergic
Primary: Percentage of Patients Reporting Adverse Events — 0.13 Percentage of Patients
Dyslipidemia
Primary: Change of Fasting Serum Low-density Lipoprotein Cholesterol (LDL-C) at 12 Weeks — 155.1; 154.6 mg/dL
Prostate Neoplasms
Primary: Phase 1: Maximum Tolerated Dose (MTD) of Abiraterone Acetate — NA mg/day
Myopia
Primary: Visual Acuity — -0.054; -0.051 LogMAR
Myopia · Hyperopia · Contact Lens Comfort
Primary: Subjective Lens Wear Comfort — 4.3; 4.3 units on a scale
Nausea · Vomiting
Primary: Number of Participants With Postoperative Nausea and Vomiting — 28; 34 participants
Treatment of Adipose Tissue in the Thighs
Primary: Clinical Improvement in Thigh Circumference — -1.22; -0.59 centimeter
Ametropia
Primary: Objective Assessment: Ocular Response - Biomicroscopy — 1.00; NA; NA; NA units on a scale
Brain and Central Nervous System Tumors
Primary: Number of Participants With Dose-limiting Toxicity (DLT) — 0; 0; 1; 2 participants
Back Pain Lower Back
Primary: Visual Analogue Scale of Pain — 47.3; 45.2 units on a scale
Nausea · Vomiting
Primary: Number of Participants With Nausea and Vomiting — 24; 29 participants