65,437 trials
COVID-19
Primary: Time to Sustained Clinical Recovery — 13.3; 12.4 days — p=0.8786
Hereditary Angioedema
Primary: Time to Beginning of Relief Based on Visual Analogue Scale (VAS) Was Defined as the Time, in Minutes, From Time of Infusion to the Beginning of Relief. — 60 minutes
Hereditary Haemorrhagic Telangiectasia (HHT)
Primary: Number of Participants That Achieving Personal Recommended Intake of Iron — 43 Participants
Covid19
Primary: Number of Participants With Sustained Clinical Recovery — 425; 475 Participants
Atrial Fibrillation · Thromboembolism · Stroke
Primary: Primary Effectiveness Endpoint 1: Composite Rate of Stroke (Including Ischemic or Hemorrhagic), Systemic Embolism and Cardiovascular or Unexplained Death — 14.28…
Covid19
Primary: Number of Participants With Clinical Improvement of Greater Than or Equal to 2 Points Using the WHO-OSCI at Day 28 — 37; 43 Participants
Colitis, Ulcerative · Crohn Disease · Inflammatory Bowel Diseases
Primary: Number of Participants Stratified by Treatment Patterns Associated With Biologics Agents Use or Non-biological Therapy in Participants With Moderate to Severe UC and CD…
Breast Cancer · Pancreatic Cancer · Colorectal Cancer
Primary: Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) — 3; 4; 5; 7 Participants
Nonalcoholic Steatohepatitis (NASH)
Primary: Number of Participants With Treatment-related Adverse Events. — 3 Participants
Paroxysmal Atrial Fibrillation · Persistent Atrial Fibrillation
Primary: Number of Participants With Acute Success of RF Ablation After Electroanatomical Mapping With HD Mapping Catheters. — 173 Participants
Left Atrial Appendage Closure · WATCHMAN Device Implantation
Primary: Comparison of Thrombin Induced Platelet-fibrin Clot Strength (TIP-FCS) Between Patients With and Without Device Related Thrombosis (DRT) Assessed at 1-year of Watchman…
Systemic Lupus Erythematosus · Lupus Erythematosus, Systemic
Primary: Number of Participants Who Experience at Least One Treatment-emergent Adverse Event (TEAE) and Serious Adverse Event (SAE) — 3; 4; 6; 2 Participants
Chronic Insomnia
Primary: Total Number of Capsules Taken During Discontinuation From Either Active Drug vs Placebo Over a Two Week Period — 0.43; 2.6; 6.3 Total number capsules chosen — p==0.05
Parkinson Disease
Primary: Change in Motor Function — -19.9 units on a scale
Sunscreening Agents
Primary: Mean Change From Baseline in Corneometer Measurements — 23.5; 24.2; 2.4; -0.6 Arbitrary units — p=<0.0001