Postoperative Complications of Ankle Arthroscopy
Recruiting now · Not applicable
Conditions studied: Ankle Injuries and Disorders, Surgery Complications
In brief
The goal of this clinical trial is to describe complications that occurred in the year following surgery, based on follow-up surgical consultations and physical therapy sessions. The target population is any adult patient who has undergone ankle surgery performed under arthroscopy. Primary outcome is description of all complications occurring within one year following ankle arthroscopy. This description will be based on clinical and functional examinations performed by surgeons and physical therapists. Participants will be regularly monitored by the surgeon and physical therapist (15 days postoperative, 3 months, 6 months, and 1 year). They will complete self-assessment questionnaires and undergo functional physical therapy tests, including ALR RSI, FAAM AVQ, FAAM Sport, CAIT, and Ankle Go.
Key facts
- Study ID
- NCT07335133
- Run by
- Clinique Saint Jean, France
- People needed
- 150
- Starts
- 2026-01-05
- Expected to finish
- 2028-06-01
- Last updated by the study team
- 2026-01-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult patient who has been informed and has signed the consent form
- Patient scheduled for arthroscopic ankle surgery.
- Patient affiliated with or covered by a health insurance plan
You may not qualify if…
- Recent traumatic injury (less than 1 month old), physical therapy assessment impossible
- Inability to follow up for up to one year
- Patient under legal protection
- Pregnant woman, patient under guardianship or conservatorship
- Patient who has already undergone ankle surgery
Where it is running
- Clinique St jean sud de france — Montpellier, France (enrolling)
Full record on ClinicalTrials.gov
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