17,261 trials
Hemorrhage
Primary: The Amount of Hemorrhage During Cesarean Delivery and Within 2 Hours Afterward — 260; 380 ml
Carcinoma, Renal Cell
Primary: Overall Response by RECIST Criteria — 3; 75; 101; 24 participants
Melanoma
Primary: Overall Best Response — 10; 1; 9; 31 participants
Advanced Breast Cancer
Primary: Percentage of Participants With Progression Free Survival (PFS) at Week 24 — 69.4; 73.5 Percentage of participants
Nausea
Primary: Five-day Nausea Diary — 2.0; 2.1; 2.1; 1.9 Units on scale — p=0.932
Chronic Obstructive Pulmonary Disease
Primary: Trough Forced Expiratory Volume in 1 Second (FEV1) Following 7 Days of Treatment — 1.317; 1.333; 1.374; 1.385 Liters
Chronic Obstructive Pulmonary Disease (COPD)
Primary: Safety of Treatment With NVA237 in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD) — 26; 26; 24; 3 Participants
Non-small Cell Lung Cancer
Primary: Overall Survival (OS) of Patients Receiving Pralatrexate vs. Erlotinib — 6.7; 7.0 Months Survival
Diabetic Macular Edema
Primary: Difference Between the Baseline Level of Visual Acuity (Letters) of the Study Eye and the Mean Visual Acuity Averaged Over All Monthly Post-baseline Assessments From…
Sickle Cell Disease
Primary: Number of Participants With Adverse Events After Start of ICL670 — 131; 49; 1; 2 participants
Alkaptonuria
Primary: Change in Total ROM Worse Hip — -9.1; 1.6 degrees
Osteoporosis
Primary: Number of Participants With Improvement in Bone Mineral Density (BMD) of Spine After Therapy — 10; 9 participants
Bloodloss · Surgical Procedures, Operative
Primary: Cumulative Volume of Packed Red Blood Cells Transfused — 1223.2; 623.5 mL — p=0.001
Falciparum Malaria
Primary: Parasitological Success Defined as a Reduction in Parasite Count of ≥ 90% of Baseline at 24 Hours After the First Dose — 14; 10 participants — p=0.17
Hidradenitis Suppurativa
Primary: 50% Reduction in Physician's Global Assessment Score (Percent of Participants) — 20 percentage of participants