6,678 trials
Penicillin Allergy · Pediatric Emergency Medicine
Primary: Number of Oral Amoxicillin Challenge Participants Completing Challenge With Insignificant Adverse Result — 114; 2 Participants
Rotator Cuff Injury
Primary: Average Postoperative Pain Scores Over a 96 Hour Timeframe — 3.0; 3.5 score on a scale
Symptomatic Irreversible Pulpitis
Primary: VAS Scores as Measures of Profoundness of Pulpal Anesthesia — 3.1; 1.2 Score on a scale
Anesthesia
Primary: Propofol Requirements With Pre-treatment of Dexmedetomidine With Children Who do Not Receive Dexmedetomidine. — 0.4; 0.23 mg/kg/min
Squamous Cell Carcinoma of Head and Neck
Primary: Objective Response Rate (ORR) — 48.5 Percentage of Participants
Primary Hypercholesterolemia
Primary: Percent Change From Baseline in LDL-C During Each Treatment — 3.4; -0.7 Percent change from baseline
Depression · HIV · AIDS
Primary: Natural Killer Cell Activity, Measured in Lytic Units [Bryant J, Day R, Whiteside TL, and Herbeman RB: Calculation of Lytic Units for the Expression of Cell-mediated…
Female Urogenital Diseases · Vaginal Atrophy · Postmenopausal Atrophic Vaginitis
Primary: Quantitative Change in Relative Abundance of Lactobacillus Among the Community Composition of Bacteria in the Vagina — 0.07; 0.09; 0.12; 0.04 Relative abundance
Tobacco Use
Primary: Number of Participants Who Report Post-treatment Satisfaction — 15; 10 Participants
Myocardial Infarction · Thrombosis · Platelet Dysfunction
Primary: Change in Maximal Platelet Aggregation in Response to Clopidogrel — 32.6; 50.8; 35.0 Percent Maximal Platelet Aggregation — p=<0.001
Schizophrenia Spectrum and Other Psychotic Disorders
Primary: Change in Biomarkers of Treatment Response: Dorsal Caudate (DCA) Gamma Amino Butyric Acid (GABA) Levels — -0.65; .0037 institutional units — p=<0.01
Healthy
Primary: Setmelanotide Concentration-related Placebo-corrected Change From Baseline (CHFB) in Fridericia's Correction (QTcF) at Day 10 — 1.9; -1.5; -3.6; -3.5 milliseconds (msec)
Pain · Quality of Life · Injection Site Reaction
Primary: Number of Participants With at Least One Severe (Grade 3) Solicited Local or Systemic Reactogenicity Event After Dose 1 of RZV (SHINGRIX®) in Each Study Group — 115…
Hepatitis C · Human Immunodeficiency Virus
Primary: The Change in Hepatitis C Viral Load From Baseline to 4 Weeks of Maraviroc or No Maraviroc — 2035071; 2027648; 2082302; 1216383 International Units/ml — p=0.13
Attention-Deficit/Hyperactivity Disorder (ADHD)
Primary: Incidence of Adverse Events During 8 Weeks of Adjunct SPN-812 Treatment — 55.4 percent of subjects