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Clinical Trial Summary

Patients who present to our institution with a traumatic injury to their elbow who need operative management will be randomized to one of two groups; a treatment arm and a control arm. The treatment arm will receive a three-week postoperative course of indomethacin while the control group will not. We will follow both groups to assess whether or not indomethacin prophylaxis affects the rate of heterotopic ossification.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01744314
Study type Interventional
Source Lawson Health Research Institute
Contact George Athwal, MD
Phone 519-646-6100
Email <gathwal@uwo.ca>
Status Recruiting
Phase N/A
Start date November 2012
Completion date November 2019