Postoperative Complications of Ankle Arthroscopy
ARTHRO2025
Short- and Medium-term Postoperative Complications of Ankle Arthroscopy
1 other identifier
interventional
150
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 5, 2026
CompletedStudy Start
First participant enrolled
January 5, 2026
CompletedFirst Posted
Study publicly available on registry
January 12, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2028
January 12, 2026
January 1, 2026
1.4 years
January 5, 2026
January 5, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
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.
One year
Study Arms (1)
Cohort of patients who underwent ankle arthroscopy
OTHERInterventions
Additional physical therapy and surgery tests and scores are performed on patients.
Eligibility Criteria
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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Clinique St jean sud de france
Montpellier, 34430, France
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 5, 2026
First Posted
January 12, 2026
Study Start
January 5, 2026
Primary Completion (Estimated)
June 1, 2027
Study Completion (Estimated)
June 1, 2028
Last Updated
January 12, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share