65,437 trials
Type 1 Diabetes
Primary: Insulin Sensitivity by Hyperinsulinemic Euglycemic Clamp — 3.27; 3.46 mg/kg/min
Type 1 Diabetes Mellitus
Primary: Adverse Events — 5; 6; 10; 4 Number of AE
Severe Acute Respiratory Syndrome · Respiratory Failure · Acute Respiratory Distress Syndrome
Primary: PaO2/FiO2 Change (Increase) From Pre-to-post Intervention — 16.9; 29.8 percent change
Coronary Disease · Coronary Stenosis
Primary: MACCE — 80; 51 Participants — p=0.35
Anxiety Disorders
Primary: Maximum Observed Plasma Concentration (Cmax) of Paroxetine — 8.39; 8.83 Nanograms per milliliter
Major Depressive Disorder · Cognitive Change
Primary: Cognition Measured Using the THINC-it Tool — -0.05; -0.12; 0.12; 0 z-score
Oropharynx Cancer
Primary: Change in Quality of Life From Mucositis-related Pain Measured by the Patient-Reported Oral Mucositis Symptoms (PROMS) Scale From Baseline to Follow-up — 20.1; 29.1…
HIV · Hepatitis C
Primary: Reactive Hyperemia Index (RHI) by Peripheral Arterial Tonometry (PAT) — 1.98; 2.15 ratio
Lung Cancer
Primary: Changes in Telemonitor Data From Baseline: Temperature — 97.05 Degrees Fahrenheit
Lymphangioleiomyomatosis (LAM)
Primary: Number of Participants With Adverse Events as a Measure of Safety and Tolerability — 11 Participants
Plaque Psoriasis
Primary: Percentage of Participants Who Achieved an sPGA Score of Clear (0) or Almost Clear (1) at Week 16 — 43.7 percentage of participants
Type 2 Diabetes Mellitus
Primary: Change From Baseline in Hemoglobin A1c (HbA1c) (10 mg and 15 mg) — -2.20; -2.37; -1.34 Percentage of HbA1c — p=<0.001
Ovarian Neoplasms
Primary: Progression Free Survival (PFS) Rate — 62 Percentage of participants
Portal Hypertension · Liver Cirrhosis
Primary: Safety (Incidence and Severity of Adverse Events) — 23; 2 Number of adverse events
Dry Eye Syndrome
Primary: Ocular Discomfort Scale — -0.6; -0.6 units on a scale