Long-term Evaluation of Sports Activity in Patients Whose Ankle Was Treated by Anatomical Reconstruction or Arthroscopic Repair Following Chronic Lateral Instability
Condition(s) studied
Investigational drug(s) / intervention(s)
Anatomical reconstruction: Anatomical ligamentoplasty or anatomical reconstruction is performed under arthroscopy. The principle of this method, which lasts around 40 minutes under spinal anaesthetic or general anaesthetic, is to reconstruct the LTFA and sometimes also the LCF, if it has been damaged, using a fragment of the tendon gracilis, located in the thigh, removed through an incision under the knee
Broström anatomical repair: Broström's anatomical repair is performed under arthroscopy. The principle of this method is to tighten and reattach the LTFA using very small anchors, when it is detached from the fibula but not too retracted and still of good quality. If necessary, this may also be accompanied by ligament reinforcement ('gould'), using a fragment of a fibrous structure in the ankle, the extensor retinaculum
Study summary
The goal of this clinical trial is to compare at 5 years the sporting activity of patients whose ankle had been treated by reconstruction or repair following chronic lateral instability. The main question it aims to answer is:
What is the long-term sporting activity status of patients whose ankle had been treated by reconstruction or repair following chronic lateral instability ?
Participants will visit the clinic once every year during 5 years for clinical checkup.
Eligibility
Primary outcome measure(s)
- Sporting activity — Year 5
Patients' sporting activity will be assessed using the "Sport" subscale of the Quick FAAM (Foot and Ankle Ability Measure) questionnaire. Minimum value is 0 and maximum value is 32. 32 means a better outcome.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Hôpital Privé Jean Mermoz | Lyon | France | Recruiting |
More GCS Ramsay Santé pour l'Enseignement et la Recherche trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06945198 on ClinicalTrials.gov ↗ ← All trials in France