65,437 trials
Adolescent Idiopathic Scoliosis · Posterior Spinal Fusion
Primary: Estimated Blood Loss/Level — 35.21; 38.68 mL
Ischemic Stroke
Primary: Number of Participants Assessed for Revascularization With mTICI Grades 2b-3 — 724 Participants
Hearth Failure With Reduced Ejection Fraction (HFrEF)
Primary: Percentage of Participants on LCZ696 200 mg Bid at Month 6 — 64.6 Percentage of Participants
Breast Feeding
Primary: Change in Total Adipose Tissue Volume — 0.718; 0.901; 0.775 Litres
Post-operative Nausea and Vomiting
Primary: Mass Balance — 96.4 percent excreted
Contraception · Knowledge, Attitudes, Practice
Primary: Change in Contraceptive Knowledge Assessment (CKA) Score — 0.90; 1.6 scores on a scale — p=<0.0001
Healthy Volunteers
Primary: Number of Participants With One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration — 0; 0; 0; 0 Participants
Gastrointestinal Bleeding · Stress Ulcers
Primary: Mortality — 510; 499 Participants
All Cause Mortality · MACE
Primary: Long-term All Cause Mortality Between On-pump and Off-pump Patients. — 131; 168; 298; 342 Participants
Advanced Prostate Cancer · Prostatic Neoplasms
Primary: To Further Quantify the Risk of Cerebrovascular Events Following Sipuleucel-T Therapy for All Subjects — 1.2 events per 100 patient years
Schizophrenia · Schizoaffective Disorder
Primary: Psychiatric Hospitalization — 4965; 5247; 2385; 3093 Participants
Depressive Symptoms
Primary: Centre for Epidemiological Studies in Depression Scale — -3.52 units on a scale
NeuroEndocrine Tumours
Primary: Assessment of Clinical Symptomatic Response — 77.8; 95.5; 87.5; 22.2 Percentage of Subjects — p==0.126
Infections, Meningococcal
Primary: Number of Subjects With Any Solicited Local and Systemic Adverse Events (AEs) — 0; 0; 0; 0 Participants
Tuberculosis
Primary: Number of Participants With Concordant CST001 Assay Results for All Replicates Across Three Testing Sites — 32; 23 Participants