65,437 trials
Contraception
Primary: Medroxyprogesterone Acetate (MPA) Concentrations — 0.00; 0.27; 0.43; 0.44 ng/mL
Mycoses
Primary: Percentage of Participants With Complete Response (CR) or Partial Response (PR) by 12 Weeks or End of Treatment — 26; 46 Percentage of participants
Tinea Pedis
Primary: Effective Treatment Outcome (Direct Microscopy and Culture Negative and Total Signs and Symptom Score Less or Equal to 2) — 73; 10 participants
Severe Asthma · Moderate or Severe Major Depressive Disorder
Primary: HAM-D (Hamilton Rating Scale for Depression) — 24.8; 28.3 units on a scale
Diabetes
Primary: MARD (Mean Absolute Relative Difference Between BGMS Results and Reference Method Results) Across the Overall Tested Glucose Range — 3.3; 4.9; 5.8; 10.7 Percent Difference
Colon Cancer
Primary: Efficacy - Preparation Quality Using a 4 Point Scale — 94; 94 percentage of participants
Chronic Pain · Opioid Induced Constipation
Primary: Incidence and Severity of Treatment Emergent Adverse Events on Single Dosing. — 8; 5; 4; 6 participants
Type 2 Diabetes Mellitus · High HbA1c Level · Inadequate Glycaemic Control
Primary: Adjusted Mean Change From Baseline in HbA1c Levels — -0.17; -0.86 Percent — p=<0.0001
Heart Failure, Congestive · Edema
Primary: Body Weight — -0.53; -1.62; -1.35; -1.85 Kg — p=0.0074
Pulmonary Hypertension
Primary: Maximum Change From Baseline in Supine Systolic Blood Pressure (SBP) Within 4 Hours Post-dose at Visit 6 (Week 12) — -20.70; -20.20 mmHg
Urea Cycle Disorders
Primary: Rate of Adverse Events During the Switchover Part of the Study Rate of Adverse Events (Number of Participants Showing Adverse Events) — 4; 2 participants
Pulmonary Disease, Chronic Obstructive
Primary: Variability in Daily FEV1, Estimated by Coefficient of Variation — 0.081; 0.079; 0.059; NA Liters
Osteoporosis, Postmenopausal
Primary: Mean Percent Change From Baseline in Bone Mineral Density at the Lumbar Spine at Month 6 — 4.26; 1.20 percent change — p=<0.0001
Abscess · Wound Infection · Surgical Site Infection
Primary: Early Clinical Efficacy — 240; 233; 48; 52 participants
Myopia
Primary: Visual Acuity — -0.029; -0.043 logMAR