Postoperative Complications of Ankle Arthroscopy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorClinique Saint Jean, France
About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
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
Trial design
Treatments tested in this trial
- Physical therapy and surgery tests and scores
Treatment groups
150 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov