65,437 trials
Smoking Cessation
Primary: Quit Attempts — 26; 33; 29; 31 Participants — p=0.07
Acute Coronary Syndromes
Primary: The Rate of International Society on Thrombosis and Haemostasis (ISTH) Major or Clinically Relevant Non-Major (CRNM) Bleeding With Apixaban Versus Vitamin K Antagonist…
Obstructive Sleep Apnea (OSA)
Primary: Apnea Hypopnea Index (AHI, Events/Hour of Sleep) — 33; 20.4 events/hour of sleep — p=0.47
Chronic Migraine or Episodic Migraine
Primary: Change From Baseline in Monthly Migraine Days to the Last 4 Weeks of the 12 Week Double-Blind Treatment Period — -2.45; -2.20; -2.19 days — p=0.66
Asthma
Primary: Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) — 40; 0 Participants
Anxiety Disorders
Primary: Hamilton Anxiety Rating Scale — 5; 6 Participants
Multiple Myeloma
Primary: Percentage of Participants With Stringent Complete Response (sCR) — 32.0; 42.4 Percentage of participants
Persistent Atrial Fibrillation
Primary: Freedom From Procedure-related Serious Adverse Events (SAEs) Within 7-10 Days of the Procedure — 92.7; 88.9 % of participants — p=0.2179
Breast Cancer
Primary: Mean Change in Bone Resorption: NTX (N-terminal Telopeptide) — NA nmol
NSCLC · Gastric Cancer
Primary: Dose-Escalation Phase: Number of Participants With Dose-Limiting Toxicity (DLT) — 0; 0; 0; 1 Participants
Stress Urinary Incontinence
Primary: Primary Effectiveness Endpoint — 107; 50 participants
Hodgkin Disease · Non Hodgkin Lymphoma · Lymphoepithelioma
Primary: Dose Limiting Toxicity (DLT) Rate by the NCI Common Toxicity Criteria (CTCAE) v2.0 and the Method of Przepiorka et al (Protocol Appendix I) — 0; 0; 0; 0 proportion of…
ST Segment Elevation Myocardial Infarction · Percutaneous Coronary Intervention
Primary: Platelet Reactivity Measured by VerifyNow PRU — 63; 214 P2Y12 reaction units (PRU) — p=<0.001
Obesity · Overweight
Primary: Percent Change From Baseline in Body Weight at 24 Weeks — -1.24; -2.04; -3.52; -4.37 Percent change — p=<0.0001
Labor Induction
Primary: Time Of Start Of Induction Of Labor To Delivery — 21.6; 26.6 hours