drugset / Trial / NCT06333522

Losartan Use to Mitigate Arthrofibrosis Following Total Joint Arthroplasty

NCT06333522

Phase 4 Withdrawn NYU Langone Health
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the effect of Losartan, an Angiotensin II Receptor Blocker (ARB), on the formation development of arthrofibrosis in patients who have had a primary total knee arthroplasty. This study aims to assess the post-operative range of motion and the incidence of MUA within three months following the index arthroplasty in the treatment arm (losartan) and the control arm.

Timeline

Start
2024-07-01
Primary completion
2026-01-01
Completion
2026-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Losartan Other / unclassified 12.5 mg Oral

Indications