6,678 trials
Procedural Sedation
Primary: Level of Sedation Throughout the Entire Procedure — 22; 9; 10; 1 participants
Cystic Fibrosis
Primary: Mean Total Administration Time — 37.0; 16.4; 4.2; 5.0 minutes
Diabetic Nephropathy
Primary: the Change of Tissue Content of Deoxyhemoglobin Assessed by BOLD-MRI — 22.04 1/ms
Coronary Artery Disease · Drug Interaction Potentiation
Primary: Comparing Platelet Function of Patients on Dual Antiplatelet Therapy With ASA + Clopidogrel, Between the Groups Ranitidin and Omeprazole, After One Week of Randomized…
Pain
Primary: Pain — 0.70; 0.88; 1.04; 0.87 units on a scale
Fungal Infection
Primary: Number of Participants With Treatment Failure — 1; 5 participants
Attention Deficit Hyperactivity Disorder
Primary: Effect of Adjunctive INTUNIV Extended Release Treatment on Executive Function as Assessed by Change From Baseline on the BRIEF-parent Questionnaires — -5.3; -6.9 units…
Cystic Fibrosis
Primary: The Use of the Approved US TOBI Podhaler Instructions for Use (IFU) to Communicates the Information Necessary to Achieve Safe and Effective Use of the Podhaler Device…
Human Immunodeficiency Virus (HIV) · HIV Associated Neurocognitive Disorders (HAND)
Primary: Change in Neurocognitive Functioning — -0.94; -0.81; -1.03; -0.51 Global Neurocognitive Z-Score — p=0.05
Analgesia, Obstetrical · Cesarean Section
Primary: Dose of IT Morphine and IT Hydromorphone for Adequate Analgesia (Pain Score Less Than or Equal to 3) in 90% of Patients — 75; 150 micrograms
Total Shoulder Arthroplasty
Primary: Numeric Rating Scale (NRS) Pain Score With Movement — 4.5; 3.4; 4.2; 4.9 units on a scale
Healthy Lactating Women
Primary: Area Under the Curve From Time Zero to End of Dosing Interval (AUCtau) — 32.50 microgram*hour/milliliter (mcg*hr/mL)
Shoulder Injury
Primary: Duration of Sensory Blockade — 16.9; 18.2; 13.8 hours — p=0.001
Retinal Vein Occlusion
Primary: Number of Participants With Adverse Events as a Measure of Safety and Tolerability — 35; 28; 45; 16 Participants
Hip Fracture
Primary: Number of Participants Who Received a Hospitalization Transfusion — 18; 12 participants