65,437 trials
Dry Eye
Primary: Inferior Corneal Fluorescein Staining — -0.69; -.97; -0.72 score on a scale
Anesthesia
Primary: Time to Extubation — 230.5; 242.4 Minutes
Chikungunya Virus
Primary: CHIKV SNA (Serum Neutralizing Antibody) Seroresponse Rate at Day 22 — 100.0 Percentage of participants
Mitral Regurgitation · Pulmonary Hypertension
Primary: Impaired Post-operative Functional Capacity — 35 Participants
Pancreatic Cancer
Primary: Distant Metastasis Free Survival (DMFS) — 9.8 months
Generalized Myasthenia Gravis
Primary: Percent Change From Baseline in Total IgG Levels at Day 29 (mITT Analysis Set) — -66.4; -62.2 percent — p=< 0.0001
Multiple Myeloma
Primary: Percentage of Participants With Adverse Events (AEs) — 100.0; 100.0; 100.0; 100.0 Percentage of Participants
Advance Care Planning
Primary: Percentage of Patients With Advance Care Planning Bills — 5,298; 4,920 Participants — p=0.41
Alzheimer Disease · Parkinson Disease
Primary: Percentage of Participants With Treatment-Emergent Adverse Events — 3; 5; 4; 6 Participants
Congenital Heart Disease · Periventricular Leucomalacia · Brain Development
Primary: Motor Scale of the Bayley Scales of Infant and Toddler Development-III — 90.0; 87.5; 88.7 score on a scale
Dyslipidemia
Primary: Number of Participants Who Experienced an Adverse Event — 2144; 2084 Participants
Type 2 Diabetes Mellitus · Cardiometabolic Conditions · Behavioral Health Concerns
Primary: Number of Patients With at Least 1 Hospital Readmission Within 30 Days After Enrollment — 43; 25 participants — p=0.01
Stage IV Adult Soft Tissue Sarcoma · Sarcoma,Soft Tissue
Primary: Number of Adverse Events of Grade ≥ 3 by CTCAE Criteria. — 8 events
Macular Edema
Primary: Number of Participants Experiencing at Least One Adverse Events (AEs) — 13; 7 Participants
Non Small Cell Lung Cancer · Urothelial Carcinoma · Malignant Melanoma
Primary: Adverse Events Evaluated by CTCAE 4.0 — 1; 7; 2; 0 Participants