Found 0 matching trials
Reduction of Low-value Prescribing Through Audit and Feedback
NAThe objective is to estimate the effect attributable to a primary care phar...
Location
Primary Care Research Unit of Bizkaia
A Trial Comparing the Safety and Efficacy of Semaglutide Once Weekly Versus Sitagliptin Once Daily in Japanese Subjects With Type 2 Diabetes
PHASE3This trial is conducted in Japan. The purpose is to compare the safety of o...
Location
Novo Nordisk Investigational Site
Enforced Reduction in Physical Activity and Recovery in Older Adults
NAApparently healthy and well-functioning community dwelling 70-80 year-olds ...
Location
University of Jyväskylä
Bone Marrow Transplant Using a Reduced Intensity Regimen That is Given in Two Steps
PHASE1This is a research study involving the treatment of patients with hematolog...
Location
Thomas Jefferson University
Consumption of More Ideal Food Options (COMIDA: Consumo de Opciones Más Ideales De Alimentos)
PHASE2The Mexican Consulate runs a Ventanilla de Salud (VDS) (Health Window) prog...
Status
Enrolling By Invitation
Location
Mexican Consulate's Ventanilla de Salud (VDS)
Living in Full Even With Pain Study
NAThis project will increase our understanding of the mechanisms underlying c...
Location
University of Washington, Ninth and Jefferson Building
Weight Maintenance Through Physical Activity and Social Support in Rural Middle-Aged Women
NAThe purpose of this study is to compare an technology-based weight maintena...
Location
Southeast District Health Department
Mini Incision Dynamic Hip Screw Technique
NAFemoral cervical fractures fixation with DHS plate throw 3 cm incision and ...
Location
Dr. Sayed Issa's Clinic
Phase 1 Dose Escalation, Single Dose Study to Assess Safety and Pharmacokinetics of BAX930 in Hereditary Thrombotic Thrombocytopenic Purpura (TTP)
PHASE1The purpose of this Phase 1, prospective, uncontrolled, open-label, multice...
Location
Ohio State University Medical Center
Slow-SPEED UK: A Double-Blind Randomised Feasibility Trial
NASlow-SPEED UK is an 18-month randomised, double-blind feasibility trial eva...