Clinical Trials Directory

Trials / Completed

CompletedNCT01234493

Syndesmotic Injury and Fixation in Supination-External (SE) Ankle Fractures

Syndesmotic Injury and Fixation in SE Ankle Fractures: A Prospective Randomized Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
140 (actual)
Sponsor
University of Oulu · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Accepted

Summary

The aim of our study was to determine whether transfixation of unstable syndesmosis is necessary in supination-external rotation type ankle fractures. Our hypothesis was that syndesmotic ligaments heal at the proper length after malleolar reduction and that syndesmotic transfixation is not needed in supination-external rotation fracture types.

Detailed description

A prospective randomized study comparing syndesmotic transfixation to no fixation in AO/OTA Weber B-type ankle fractures was designed. To show a clinically significant difference (Olerud-Molander ankle score 20%, standard deviation (SD) 24 points, from our previous study) between the groups, the sample size was estimated (α=0.05, β=0.2, 20% drop out) to be 30 patients per group. All skeletally mature patients (≥16 years old) with a unilateral Lauge-Hansen supination-external rotation type 4 ankle fractures treated within one week after injury at our hospital were considered eligible for the present study. Exclusion criteria were bilateral ankle fractures, pathologic fractures, concomitant tibial shaft fractures, previous significant injury or a fracture of either ankle, significant peripheral neuropathy, soft tissue infection in the region on either injured ankle, or inability to complete the study protocol. After bony fixation, the 7.5-Nm standardized external rotation (ER) stress test for both ankles was performed under fluoroscopy. A positive stress examination was defined as a difference of more than 2 mm side-to-side in the tibiotalar or tibiofibular clear spaces on mortise radiographs. If the stress test was positive, the patient was randomized to either syndesmotic transfixation with 3.5-mm tricortical screws or no syndesmotic fixation. Clinical outcome was assessed using the Olerud-Molander scoring system, RAND 36-Item Health Survey, and Visual Analogue Scale (VAS) to measure pain and function after a minimum 1-year of follow-up.

Conditions

Interventions

TypeNameDescription
PROCEDUREfixationSyndesmosis fixation with one 3.5mm fully threaded three cortical screw
PROCEDUREno fixationNo syndesmosis fixation.

Timeline

Start date
2007-06-01
Primary completion
2010-08-01
Completion
2010-08-01
First posted
2010-11-04
Last updated
2016-05-16

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT01234493. Inclusion in this directory is not an endorsement.