Actively Recruiting
Postoperative Complications of Ankle Arthroscopy
Led by Clinique Saint Jean, France · Updated on 2026-01-12
150
Participants Needed
1
Research Sites
125 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Postoperative Complications of Ankle Arthroscopy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Clinique St jean sud de france
Montpellier, France, 34430
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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