65,437 trials
Chronic Insomnia
Primary: Number of Participants Using WatchPAT — 11; 11 Participants
Polycystic Kidney, Autosomal Dominant
Primary: Percent of Participants Demonstrating 20% or More Increase in Total Kidney Volume — 69; 88 percentage of participants — p=0.03
Diabetes · Diabetes Mellitus, Type 2
Primary: Change in HbA1c From Baseline — -1.21; -1.64; -0.83 percentage — p=<0.0001
Supraventricular Tachycardia
Primary: Total Fluoroscopy Time — 18.3; 7.5 minutes
Urinary Incontinence, Urge
Primary: Number of Urge Urinary Incontinence (UUI) Episodes — -3.25; -3.89 UUI episodes
COPD
Primary: Change From Baseline in Morning Trough Forced Expiratory Volume in 1 Second (FEV1) — 0.0009; 0.1055; 0.1333; 0.1336 liters — p=0.0043
B-Cell Lymphoma
Primary: Maximum Tolerated Dose (MTD) of Inotuzumab Ozogamicin in Combination With Rituximab (375 mg/m^2 ) — 1.8 mg/m^2
Sensitivity to Dental Cements · Dental Crowns · Dental Three-unit Bridges
Primary: Incidence of Post-operative Pain (Yes/no) — 1; 0; 1; 2 participants — p=0.5637
Breast Tumor · Breast Cancer · Cancer of the Breast
Primary: Kaplan-Meier Estimates of Progression-Free Survival (PFS) Based on Investigator Assessment. — 5.5; 8.3; 6.0 months — p=0.0183
Opioid-Induced Constipation
Primary: The Proportion of Subjects Who Have a Rescue-free Laxation Response Within 4 Hours After at Least 2 of the First 4 Doses — 62.9; 9.6 percentage of participants — p=<…
Obesity
Primary: Least-Square Mean Difference in % Total Body Loss (TBL) Between the Obalon Treatment and Sham Control Groups — 6.86; 3.59 %TBL — p=0.0261
Pancreatic Cancer
Primary: FDG Therapeutic Responses to 1 Cycle — 6 participant responses based on EORTC
Sleep Apnea, Obstructive
Primary: Total Suction Electrocautery Time Required for Hemostasis Will be Recorded as Seconds — 155.3; 60.9; 94.5 seconds
Prematurity · Necrotizing Enterocolitis
Primary: Salivary EGF (Epidermal Growth Factor) Protein Levels — 15 picograms EGF/ microgram of protein
Cardiovascular Disease
Primary: Hemostasis at the Target Bleeding Site (TBS) at 3 Minutes Following Treatment Application. — 12; 6; 5 Participants