Functional and Patient-reported Outcome After Peroneal Tendon Surgery and Different Immobilization Protocols

Launched by VASTRA GOTALAND REGION · Sep 9, 2024

Keywords

ClinConnect Summary

This clinical trial is exploring the effects of different post-surgery recovery plans for patients who have undergone surgery for a peroneal tendon injury, which can occur in the ankle. The study is taking place in Gothenburg, Sweden, and aims to understand how these different recovery methods impact patients' healing and overall satisfaction with their recovery. Patients will be randomly assigned to one of two recovery plans after their surgery, and their progress will be evaluated through physical tests and questionnaires that measure their experiences and outcomes.

To participate in this trial, individuals must be between 65 and 74 years old and have had surgery for a peroneal tendon rupture or related injury. However, those who have had extensive previous surgeries in the same area, have certain medical conditions, or are under 18 years old will not be eligible. During the trial, patients can expect to undergo tests on both their injured ankle and the healthy one, providing valuable data on how well they are recovering. This study is currently recruiting participants, and it aims to help improve recovery processes for future patients.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • \* Surgery of peroneal tendon rupture and/or rupture of ligament and/or rupture of retinacle
• Exclusion Criteria:
• • Extensive surgery needed, such as for example heel osteotomy
• • Previous surgery in the affected area
• • Previous injury in the healthy foot/leg that impairs function
• • Neuromuscular disease
• • Impaired language comprehension
• • Age under 18