65,437 trials
Hemostasis
Primary: Mean Paired Kappa Statistic for the Assignment of SBSS Scores by 2 Investigators — 0.7754 Kappa statistic
Inflammatory Bowel Disease · Ulcerative Colitis · Crohn´s Disease
Primary: Medical Adherence — 23.3; 23.3 units on a scale — p=0.22
Metastatic Breast Cancer
Primary: Dose-Limiting Toxicity (DLT) of MK-3475 in Combination With Trastuzumab — 0; 0 Participants
Visceral Leishmaniosis · HIV-infection/Aids
Primary: Probability of Relapse-free Survival — 79; 71 percentage probability
Glaucoma
Primary: Number of Participants Assessed for Intraocular Pressure Change — 0; 4; 4; 8 Participants
Anesthesia, General
Primary: Time From Start of Administration of Sugammadex or Placebo to Recovery of the Fourth Twitch/First Twitch (T4/T1) Ratio to 0.9 — 96.30; 16.30; 4.62; 1.43 Minutes
Pain, Postoperative
Primary: Narcotic Use at 24 Hours Postop — 158.8; 175.0 morphine milligram equivalents
Pre Eclampsia
Primary: Accuracy of Blood Pressure Measurement by Sphygmo Relative to the Clinical Standard. — 122.5; 74.5; 123.1; 72.1 mmHg
Critically Ill · Pneumonia
Primary: Maximum Plasma Concentration (Cmax) of Ceftolozane or Tazobactam in Mechanically Ventilated Participants for the First and Last Dose of Ceftolozane/Tazobactam Treatment…
Neovascular Age-related Macular Degeneration
Primary: Change in Central Subfield Retinal Thickness (CSRT) From Baseline to Day 90. — 384.00; 318.00; -30.75 micrometer — p=<0.0001
Falls · Balance · Insomnia
Primary: Change in Balance — 6.66; 5.34; 5.62; 5.78 %CV
Fontan Circulation
Primary: The Change in Exercise Capacity Measured Via Maximum Oxygen Consumed During Exercise (VO2) — 39.4; 36.8; 41.2; 34.4 ml/min/kg
Psoriasis
Primary: Part I: Percentage of Participants Who Achieved Psoriasis Area and Severity Index (PASI) 90 Response at Week 24 — 81.7; 13.6 Percentage of Participants — p=<0.0001
Refractive Error
Primary: Incidence (Number) of Ocular Discomfort Device-related Adverse Events (AEs) — 0; 0 Eyes
Chronic Constipation · Irritable Bowel Syndrome With Constipation
Primary: Number of Participants With at Least One Treatment-Emergent Adverse Events (TEAEs) — 399; 748 Participants