65,437 trials
Cardiac Arrhythmia
Primary: Detection of Cardiac Arrhythmias — 107; 104 Participants
Suture Related Complication
Primary: The Measured Difference in POSAS and VAS Scores Between 7-day and 10-day Groups — 12.9; 16.1; 19.5; 20.3 score on a scale
Depressive Disorder, Major
Primary: Percentage Change of the BOLD Signal — -0.08; 0.43 percentage change in BOLD signal
Acute Myeloid Leukemia · Myeloid Leukemia · Monocytic Leukemia
Primary: Number of Participants Experiencing Dose Limiting Toxicity (DLT) Events — 0; 0; 0; 0 Count of Participants
Kidney Stone · Pain, Postoperative · Addiction
Primary: Visual Analog Scale of Pain Score — 3.7; 2.0 units on a scale
Cancer · Quality of Life · Anxiety
Primary: Pediatric Quality of Life Cancer Module — 66.89; 68.41 score on a scale
Underage Drinking
Primary: Acceptability (Parent)- Program Usefulness — 42 Participants
COVID-19
Primary: Number of Subjects With Sustained Resolution of COVID-19 Signs and Symptoms Without Subsequent Symptom Recurrence or Disease Progression (Until the End of the Study)…
Cutaneous Lichen Planus
Primary: Percentage of Participants Achieving Investigator's Global Assessment-Treatment Success (IGA-TS) at Week 16 — 50.0; 21.9 percentage of participants — p=0.0129
Peritoneal Carcinomatosis · Colorectal Cancer · Appendiceal Cancer
Primary: Completeness of Cytoreduction
Genetic Obesity
Primary: Stage 1: Number of Participants by Genotype Who Demonstrated a Significant Clinically Meaningful Response to Setmelanotide at the End of Stage 1 — 49; 0; 0; 2 Participants
Type 2 Diabetes Mellitus
Primary: Changes in Liver Fat — 5.4; 7.3 percent liver fat — p=0.05
Fallopian Tube Clear Cell Adenocarcinoma · Fallopian Tube Endometrioid Adenocarcinoma · Fallopian Tube High Grade Serous Adenocarcinoma
Primary: Dose-limiting Toxicities (Phase I) — 2; 3 participants
Pediatric Obesity · Meal Timing
Primary: Change in Insulinogenic Index From Baseline After Test Meal From Venous Sample — 268; 215; 153 Microunits per milliliter
Cystic Fibrosis
Primary: Safety and Tolerability as Assessed by Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Serious TEAEs — 85; 21 Participants