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RecruitingNCT06593912

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

Comprehensive Assessment of Peroneal Tendon Injuries - Evaluation and Treatment

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Vastra Gotaland Region · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Patients with surgery of a peroneal tendon injury in Gothenburg, Sweden, will be randomized to one of two different postoperative protocols. Before and after surgery the patients will perform biomechanical evaluation and also fill out questionnaires including PROMs. All evaluations will be performed on both limbs.

Detailed description

Patients admitted for surgery because of peroneal tendon injury will be randomized to one of two postoperative immobilization protocols. In group A the patients will use a cast for 6 weeks after surgery. In group B, the patients will use a cast for 3 weeks followed by a Air Stirrup for 3 weeks. The patients in group B will start unloaded range of motion 3 weeks after surgery. Both groups are allowed to weight-bear directly after surgery. The patients will be evaluated before and several times after surgery. Patient-reported outcome measures (PROMs) will be used to evaluate changes in patient quality of life between the two interventions. A biomechanical evaluation of the ankle, knee and hip kinematics and kinetics during walking, running and walking will also be performed before and repeatedly after surgery.

Conditions

Interventions

TypeNameDescription
PROCEDUREEarly Functional TrainingEarly functional training after 3 weeks using Air Stirrup compared to cast (standard protocol) after peroneal tendon surgery.
PROCEDUREStandard protocolCast 6 weeks after peroneal tendon surgery (standard protocol)

Timeline

Start date
2024-10-01
Primary completion
2027-12-31
Completion
2030-12-31
First posted
2024-09-19
Last updated
2025-09-23

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT06593912. Inclusion in this directory is not an endorsement.