Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
150 participants
INTERVENTIONAL
2026-01-05
2028-06-30
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Cohort of patients who underwent ankle arthroscopy
Physical therapy and surgery tests and scores
Additional physical therapy and surgery tests and scores are performed on patients.
Interventions
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Physical therapy and surgery tests and scores
Additional physical therapy and surgery tests and scores are performed on patients.
Eligibility Criteria
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Inclusion Criteria
* Patient scheduled for arthroscopic ankle surgery.
* Patient affiliated with or covered by a health insurance plan
Exclusion Criteria
* 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
18 Years
ALL
No
Sponsors
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Clinique Saint Jean, France
OTHER
Responsible Party
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Wayan HEBRARD
Principal Investigator
Locations
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Clinique St jean sud de france
Montpellier, , France
Countries
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Facility Contacts
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Other Identifiers
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2025-A02186-43
Identifier Type: -
Identifier Source: org_study_id
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