Stopped: Study was slow to recruit. PI decided to close study to focus on other trials.
Aim: * Determine if external fixation decreases soft tissue complications compared to splinting. * Determine if external fixation decreases time to definitive surgical stabilization and improves final fixation compared to splinting. * Determine if external fixation improves functional outcomes as evaluated by validated functional scoring systems. Hypothesis: * External fixation improves definitive fixation and functional outcomes of acute calcaneal fractures with decreased complication rates compared to splinting
Age range
18 Years – 69 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Time to Definitive Surgery
Timeframe: Within 2 weeks from injury
Soft Tissue Complications
Timeframe: Assessed at 2 weeks after surgery
Soft Tissue Complications
Timeframe: Assessed at 6 weeks after surgery
Soft Tissue Complications
Timeframe: Assessed at 12 weeks after surgery
Soft Tissue Complications
Timeframe: Assessed at 6 months after surgery
Soft Tissue Complications
Timeframe: Assessed at 12 months after surgery
Soft Tissue Complications
Timeframe: Assessed at 24 months after surgery