65,437 trials
Critical Illness
Primary: Perfused Boundary Region (PBR) in One Week — 1.95; 1.97; 2.02 micrometer
Osteoarthritis
Primary: "Worst Knee Pain" Likert Scale (0-10) Reported on Survey — 25; 35 Participants
Lower Urinary Tract Symptoms
Primary: Percentage of Participants Who Appropriately Followed the Label Instructions — 85.4 Percentage of participants
Migraine, With or Without Aura
Primary: Percentage of Participants With Freedom From Pain at 2 Hours Post-dose — 21.2; 10.9 percentage of participants — p=< 0.0001
Electrocardiogram Repolarisation Abnormality · Gonococcal Infection
Primary: The One-sided 95% Confidence Interval (CI) for the Largest Time-matched, Placebo-corrected, Baseline-adjusted Mean QTcF Interval (Delta Delta QTcF) Following…
Healthy
Primary: Reflexive Cough Testing (With Urge-to-Cough) — 3; 5 units on a scale
Schizophrenia
Primary: Evaluate Efficacy and Safety of Asenapine Maleate Patches Compared With Placebo Patches in Subjects Diagnosed With Schizophrenia as Measured Using the Syndrome Scale…
Attention-Deficit Hyperactivity Disorder (ADHD)
Primary: Change From Baseline at Day 15 in , ADHD Symptoms as Measured by Mean Swanson,Kotkin,Agler,M-Flynn, Pelham Rating Scale(SKAMP)-Combined Score Obtained From an Average of…
Postural Balance · Accidental Falls · Mobility Limitation
Primary: Balance and Lateral Mobility Assessed by the Four Square Step Test — -1.8; -0.6 seconds — p=<0.05
Acute Pain · Cesarean Delivery
Primary: Opioid Consumption — 31 milligrams of oxycodone
Pancreatic Adenocarcinoma
Primary: Individually Optimized Contrast-enhanced 4DCT for Radiotherapy Simulation — 4.1; 2.5; 3.6; 3.9 units on a scale
Schizophrenia
Primary: Plasma Concentration at 24 Hours Post-dose (C24hr) of MK-8189 in Schizophrenia Participants — 67.0; 60.5; 161; 81.1 nM
Cystic Fibrosis
Primary: To Determine the Pharmacokinetic Profile of IV (Intravenous) and PO (Oral) Formulations of Linezolid Among Children With Cystic Fibrosis
Hypertension
Primary: Change in Systolic Blood Pressure From Baseline to 6 Months on 24-h Ambulatory Measurement (Follow-up Minus Baseline Measurement) — 0.7; -21.7 mmHg — p=0.018
Prader-Willi Syndrome
Primary: Post-treatment Total Score on the Hyperphagia Questionnaire for Clinical Trials (HQ-CT) — 15.9; 14.7 score on a scale