drugset / Trial / NCT07179042

Intertrochanteric Femur Fracture Patients Who Receive Metformin With a Placebo

NCT07179042

Phase 0 Enrolling by invitation 60 enrolled University of Utah
RandomizedParallel-groupDouble-blindTreatment

Summary

The investigators central hypothesis is that metformin supplementation will be well-tolerated, safe, and provide patients with improved functional and muscle morphology outcomes following intertrochanteric femur fracture. The objectives will be tested in older adults that sustain a hip fracture and are randomized to receive a daily oral dose (1.5g daily) of metformin or a non-active placebo during 4 months of recovery following surgery.

Timeline

Start
2025-09-04
Primary completion
2030-09
Completion
2030-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Metformin Small molecule 1500 mg Oral

Indications