65,437 trials
Post-ERCP Pancreatitis
Primary: The Proportion of Subjects in Each Study Group With Post-ERCP Pancreatitis — 145; 110; 137; 90 Participants
Chronic Pain
Primary: Responder Rate — 51; 5 Participants
Lymphomas · Solid Tumors · NSCLC
Primary: Phase 2: Response Rate of This Combination in Participants With Colon Cancer, Non-small Cell Lung Cancer (NSCLC), and Granulosa Cell Ovarian Cancer — 0; 0; 0; 1…
IOP · Osteoporosis
Primary: Difference in BMD at the Lumbar Spine (L1-4) Within Group — -1.1; -2.4 percentage of change
Substance Use · Sexual Risk
Primary: Illicit Drug Use Days — 3.04; 11.62; 2.00; 6.04 days — p=.19
Cystic Fibrosis
Primary: Safety and Tolerability as Assessed by Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs) — 118; 13 Participants
Hematological Malignancies
Primary: Treatment-related Adverse Events — 4 Participants
Endothelial Dysfunction · Biochemical Markers
Primary: Inflammatory Blood-Based Biomarkers — 5 fold change — p=0.05
Recurrent Childhood Ependymoma
Primary: Objective Response Rate (Complete Response Rate and Partial Response Rate) Following Treatment With Everolimus for Children With Recurrent or Progressive Ependymomas…
Ischemic Stroke
Primary: Successful Reperfusion, Defined as mTICI Score ≥ 2b — 130 Participants
Substance Use
Primary: Feasibility: e-SBI Session 1 Completion Rate — 8; 4; 2; 0 Participants
Meningitis
Primary: Number of Participants With Seroprotection for Meningitis Serogroups A, C, W and Y — 373; 191; 366; 180 Participants
Cerebral Palsy (CP)
Primary: Status/Safety Assessment — 4; 7; 20; 12 number of sessions symptom reported
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…
Cirrhosis · Hepatic Encephalopathy
Primary: Number of Participants Who Experienced Serious Adverse Events up to Week 6 — 2; 0 Participants