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Comparing Clinical Outcomes of Suture Button Versus Fibulink Fixation for Acute Ankle Syndesmosis Injuries

Ankle Fractures Clinical Trial

Official title:
Randomized Controlled Trial Comparing Clinical Outcomes of Patients Treated Surgically with Suture Button Versus Fibulink Fixation for Acute Ankle Syndesmosis Injuries

Clinical Trial Summary

This project consists of a randomized controlled study design. Study candidates will include all patients 18 years or older, who were evaluated at UCSD and found to have an acute ankle syndesmosis injury requiring surgery. Patients who consent to study participation will be randomized to receive one of two standard of care procedures - either a suture button or Fibulink implant. Outcome measures, including the Olerud-Molander and American Orthopaedic Foot and Ankle Society scores, pain, range of motion, time to return to work, and radiographic evaluation will be collected for each participant. Given the potential degenerative changes and poor radiographic and clinical outcomes with inadequate repair of the syndesmosis, it is imperative to evaluate existing and emerging methods of fixation for patients with acute ankle fractures with syndesmosis injuries.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05729542
Study type Interventional
Source University of California, San Diego
Contact Dominic Baun, MS
Phone 858-534-8268
Email jbaun@health.ucsd.edu
Status Recruiting
Phase N/A
Start date November 18, 2021
Completion date November 18, 2027
View Details
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