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Clinical Trial Summary

This study is a multicenter prospective randomized control trial comparing hardware retention (HR) to removal of hardware (RH).


Clinical Trial Description

Eligible patients will be randomized to one of two treatment arms: Hardware removal at 6 months or Hardware retention for a minimum of 2 years. Consenting patients having previously undergone open reduction and internal fixation of Lisfranc injuries with an anatomic reconstruction within 6-8 weeks will be randomized to one of two treatment arms: removal hardware (RH) or hardware retention (HR). Outcome will be assessed at 6 weeks, 12 weeks, 6 months, 1 year, and 2 years from enrollment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02374944
Study type Interventional
Source University of Calgary
Contact Karin Lienhard, PhD
Phone 403-944-2932
Email karin.lienhard@ucalgary.ca
Status Recruiting
Phase N/A
Start date January 23, 2018
Completion date December 2025