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NOT YET RECRUITING
NCT07685743
PHASE4

Extended Post-operative Oral TXA in Primary THA

Sponsor: Oregon Health and Science University

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to learn if extended post-operative oral tranexamic acid (TXA) - a medication that reduces bleeding by slowing the breakdown of blood clots - can improve functional recovery following surgery in adults undergoing primary total knee or hip arthroplasty for osteoarthritis. The main question it aims to answer is: Does extended post-operative oral TXA improve functional outcomes at 6 weeks post-operatively compared to standard perioperative TXA alone? Researchers will compare patients receiving extended oral TXA to patients receiving matching placebo capsules on the same schedule to see if the extended TXA regimen reduces blood loss, improves early functional outcomes, and reduces pain without increasing complication rates. Participants will receive standard perioperative oral TXA (1.95 g) prior to surgical incision, along with standard VTE prophylaxis. They will be randomly assigned to receive either oral TXA or matching placebo capsules once daily on post-operative days 1, 2, and 3. Participants will attend follow-up visits at 2, 6, and 12 weeks post-operatively to complete functional outcome questionnaires, pain assessments, and - for knee replacement patients - range of motion measurements.

Official title: Extended Post-operative Oral TXA vs.Standard Perioperative TXA in Primary TJA: A Randomized, Double-Blind, Placebo-Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

170

Start Date

2026-09-01

Completion Date

2028-09-01

Last Updated

2026-07-08

Healthy Volunteers

No

Interventions

DRUG

Extended oral tranexamic acid regimen

Participants in the intervention group will receive 1.95mg of oral tranexamic acid on post-operative day 1, 2, and 3.

DRUG

Placebo

Patients will receive an oral placebo medication on post-operative day 1, 2, and 3.