Ankle Injuries and Disorders, Surgery Complications
Conditions
Brief summary
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.
Interventions
Additional physical therapy and surgery tests and scores are performed on patients.
Sponsors
Study design
Eligibility
Inclusion criteria
* 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
Exclusion criteria
* 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Complications occurring within one year following ankle arthroscopy | One year | 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. |
Countries
France