Postoperative Complications of Ankle Arthroscopy

Clinique Saint Jean, France150 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

OTHER

Masking

NONE

Enrollment

150

Conditions

Ankle Injuries and Disorders Surgery Complications

Interventions

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Outcomes

Primary Outcomes

Complications occurring within one year following ankle arthroscopy

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.

Time frame: One year