drugset / Trial / NCT07494032

Extended Oral Tranexamic Acid After Primary Total Knee Arthroplasty

NCT07494032

Not yet recruiting 350 enrolled NYU Langone Health
RandomizedParallel-groupQuadruple-blindSupportive care

Summary

This study is a prospective double-blind randomized controlled trial to evaluate the effect of extended oral TXA after primary total TKA on short-term and mid-term postoperative outcomes, including function, pain, and postoperative complications over a 24-month period, with evaluations at 6 weeks, 3 months, 12 months, and 24 months. Each group of 175 patients will receive either extended oral TXA 1.95g daily or placebo for 7 days postoperatively. Function will be assessed by Knee Injury and Osteoarthritis Outcome Score, Joint Replacement (KOOS, JR) scores measured at all post operative time points as well as range of motion (ROM) (measured at all visits).

Timeline

Start
2026-05-01
Primary completion
2029-05-01
Completion
2029-05-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Tranexamic Acid Small molecule 650 mg Oral

Indications