Tranexamic Acid vs. Quixil - Reducing Blood Loss in Joint Replacement

Not Applicable

Completed

• Conditions: Hemorrhage; Arthroplasty, Replacement, Hip; Arthroplasty, Replacement, Knee

• Registration Number: NCT00378872
• Lead Sponsor: Golden Jubilee National Hospital

Brief Summary

We will compare the effectiveness of Quixil and Tranexamic acid in reducing bleeding during hip and knee joint replacements.

Detailed Description

This is a prospective randomised controlled trial to compare the benefits of Quixil vs. Tranexamic acid in reducing blood loss.

Both medicines are used for the reduction of blood loss in major joint surgery; previous studies have shown each one to be effective and safe, but they have not been directly compared in this setting.

We will compare the blood loss in each of 3 groups: tranexamic acid used, Quixil used, and control group (neither drug used). Blood loss is to be calculated from height, body weight and difference between pre and post-operation haematocrit.

Study Timeline

• Study Start: 2006-06
• Study First Submitted: 2006-09-20
• Study First Submitted QC: 2006-09-20
• Study First Posted: 2006-09-21
• Status Verified: 2008-05
• Primary Completion: 2008-05
• Study Completion: 2008-05
• Last Update Submitted: 2008-05-13
• Last Update Posted: 2008-05-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 132

Inclusion Criteria

• Patients who are to undergo elective hip or knee joint replacement
• Must be cemented arthroplasty
• Must be primary arthroplasty

Exclusion Criteria

• Uncemented arthroplasty.
• Revision arthroplasty.
• Patients on anticoagulant (warfarin, low molecular weight heparin) or other medication known to affect clotting (except aspirin, which is to be given as part of standard DVT prophylaxis in all cases).
• Other drugs that may affect the activity of the drugs under investigation.
• Allergy to asprin (all patients to receive 150mg aspirin as standard DVT prophylaxis for 6 weeks).
• Patients with known coagulopathy (APTT or PT outside normal range pre-operatively).
• Previous reaction or ethical/religious objection to receiving blood products (Quixil contains a derivative of human blood).
• Pregnancy or breastfeeding.
• Patients who have a past medical history of thrombo-embolism at any time.
• Patients who need intravenous fluid administration for greater than 24 hours following operation.
• Patients who need allogenic blood transfusion within study period.
• Jehovah's Witnesses, or any other group of patients with ethical objections to receiving blood products.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Blood loss as calculated from change in haematocrit

Trial Locations

Locations (1)

Golden Jubilee National Hospital; 🇬🇧 Clydebank, Scotland, United Kingdom