65,437 trials
PAD
Primary: Change of Ankle Brachial Index (ABI) at 6-month Post-procedure. — 0.24; 0.44 ratio
Giant Cell Tumor of Bone
Primary: Number of Participants Experiencing Adverse Events (AEs) of Interest (EOI) — 3; 0; 6; 1 Count of Participants
Depressive Symptoms
Primary: Change in the Quick Inventory of Depressive Symptoms-Self Report (QIDS-SR) — 13.67; 14.09; 14.29; 13.79 units on a scale — p=.54
Opioid Withdrawal
Primary: Subjective Opioid Withdrawal Scale-Gossop (SOWS) Scale Score — 7.0; 9.1 score on a scale — p=.05
SARS-CoV-2 Infection
Primary: Participants With Adverse Events (AEs) up to 72 Hours Post-dosing — 2; 1; 2 Participants
Respiratory Syncytial Virus
Primary: Panel A vs Panel C: Peak Viral Load (PVL) Determined by Viral Quantitative Culture — 2.55; 2.84 log10 plaque forming units (PFU)/mL — p=0.578
Chordoma
Primary: Overall Response Rate — 1; 1 Participants
Effects of Immunotherapy · Metastatic/Recurrent Cervical Cancer · Cervical Adenocarcinoma
Primary: Number of Participants With Dose Limiting Toxicities (DLTs) — 0; 1; 0 Participants
Human Immunodeficiency Virus Transmission · Sexually Transmitted Diseases
Primary: PrEP Prescriptions (As Measured by Chart Review) — 1; 0 Participants — p=0.51
Pre-Eclampsia
Primary: Folate Status — 2701; 2686; 105; 67.1 nmol/L
Diabetes Mellitus, Type 2 · Hypoglycemia
Primary: Change in Mean Glucagon Concentration During Induced Hypoglycemia From Target Plasma Glucose (PG) Concentration of 100 Milligrams Per Deciliter (mg/dL) to a Nadir Target…
Non-valvular Atrial Fibrillation
Primary: Incidence Rate (Per 1,000 Participant-Year) of Composite of Stroke and Systemic Embolism (SE): Balanced Cohorts — 75.227; 55.801 Events Per 1000 Participant-Years…
Venous Leg Ulcer
Primary: Time to Ulcer Healing From Date of Randomisation to Date of Healing up to 365 Days — 82; 56 days
Myelodysplastic Syndromes
Primary: Number of Participants Evaluated for Hematologic and Nonhematologic Toxicities as Measured by NCI CTC v2.0 — 5; 14; 7; 28 Participants
RSV Infection
Primary: Number of Participants With Unsolicited Treatment Emergent Adverse Events (TEAEs) Through Day 151 — 1; 2; 3; 3 Participants