65,437 trials
End-stage Liver Disease (ESLD) · Liver Transplant · Sarcopenia
Primary: Physical Fitness - VO2 — -1; -3 mL oxygen/kg/min — p=0.49
Diabetes Mellitus, Type 1
Primary: Time in Range (%) — 64 percentage of time (minutes)
Anesthesia
Primary: Requirements of the Inhalational Anesthetic Desflurane, Measured in Expiratory Volume Percentage, to Maintain a BIS-Index Triggered Depth of Anesthesia — 3.6; 3.7…
Pain, Postoperative
Primary: Postoperative Pain (Pain Scores) Intensity Measure — 1; 3 units on a scale — p=0.001
Lymphoma, Large Cell, Diffuse
Primary: Percent of Participants With Progression Free Survival (PFS) After 1 Year Treatment — 16.4 percentage of participants
Pain
Primary: Change in Patient-reported Worst Pain Between Baseline and 5 Weeks of Treatment With Duloxetine — 6.54; 0.25; 4.06 score on a scale
Human Immunodeficiency Virus
Primary: Number of Participants With Severe and Life-threatening Adverse Events (AEs) — 0; 4; 4; 0 Participants
Heart Failure, Congestive
Primary: Efficacy Endpoint: Ventilatory Anerobic Threshold (VAT) — 28; 38 Participants — p=0.31
Visual Acuity
Primary: Non-Invasive Break Up Time (NIBUT) or Non-Invasive Keratograph Break Up Time (NIKBUT) — 8.28; 11.10 Seconds
Asthma
Primary: Change From Baseline in Forced Expiratory Volume in One Second (FEV1) — 0.043; 0.016 Liters — p=0.7374
HIV
Primary: Sexual Pleasure Scale Score for Fitted Versus Standard Condoms — 71.52; 70.13 score on a scale — p=<0.05
Oxygen Deficiency · Desaturation of Blood · Hypoventilation
Primary: Number of Surgical Interruptions — 0.645; 0.302 Interruptions — p=0.206
Colonic Neoplasms
Primary: Percentage of Participants With Progression Free Survival (PFS) at 6 Months — 27.50 percentage of participants
Pulmonary Disease, Chronic Obstructive
Primary: Percentage of Participants That Reported COPD Symptom Burden- Measured Using COPD Assessment Test (CAT) Questionnaire — 13.27; 11.34; 51.28; 43.58 Percentage of…
Glaucoma
Primary: Postoperative Intraocular Pressure Changes Between Targeted Supratenon's Placement of XEN-45 Gelatin Stent and Nontargeted Placement. — 20; 15 Participants