Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT06384456

Topical TRanexamic Acid vs. Placebo on Acute Postoperative Pain Following DRF Fixation

Led by University Health Network, Toronto · Updated on 2026-05-04

90

Participants Needed

1

Research Sites

120 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this study is to find out whether the use of topical tranexamic acid (TXA) into the surgical wound will result in less post-operative pain, less pain killer use, and better post-operative use of the wrist in people undergoing surgery for a wrist fracture compared to not using topical TXA (placebo).

CONDITIONS

Official Title

Topical TRanexamic Acid vs. Placebo on Acute Postoperative Pain Following DRF Fixation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing open reduction internal fixation (volar approach) for distal radius fracture surgery
  • Age 18 years or older
  • Able to provide informed consent
  • Cognitive ability and English language skills to complete outcome measures
Not Eligible

You will not qualify if you...

  • Revision surgery or additional operations on the same wrist
  • Distal radius fracture treated with dorsal surgical approach
  • History of lymphedema or lymph node removal in the affected arm
  • Known chronic pain conditions such as fibromyalgia or polymyalgia rheumatica
  • Current or chronic use of opioids
  • Known allergy to tranexamic acid
  • Anticoagulant medications not stopped according to guidelines
  • Previous thrombotic stroke or blood clotting disorders
  • Current pregnancy or breastfeeding
  • Previous neurologic injury causing paralysis of the affected shoulder or arm
  • Severe heart or lung disease (ASA Grade IV or higher)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Toronto Western Hospital

Toronto, Ontario, Canada

Actively Recruiting

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Research Team

R

Ryan Paul

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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