Actively Recruiting
Anterior Cruciate Ligament (ACL) Revision Surgery: French National Study
Led by Centre Hospitalier Universitaire de Saint Etienne · Updated on 2024-07-22
300
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate clinical practice in anterior cruciate ligament (ACL) revision surgery across multiple centers in France. Led by the French Arthroscopy Society and sponsored by the Centre Hospitalier Universitaire de Saint Etienne, the study focuses on collecting epidemiological, morphological, operative data, as well as clinical and functional outcomes and surgical complication rates in patients undergoing ACL revision surgery. Patients who have had an ACL revision surgery, which involves replacing the ACL graft with a new one, will be included. Data collection includes questionnaires such as the Anterior Cruciate Ligament Return to Sport and Injury (ACL-RSI), Tegner Activity Scale (TAS), Simple Knee Value (SKV), and International Knee Documentation Committee (IKDC) scores at 0, 6, 12, and 24 months. Medical record data including surgical details, complications, and functional outcomes will also be gathered. Participants will complete the listed questionnaires multiple times over two years to assess knee function and activity levels. Researchers will monitor surgical complications from the time of surgery up to two months. The study's primary measurements include functional scores related to knee performance and return to sport, with follow-up assessments extending to 24 months after surgery.
CONDITIONS
Brief Title
Anterior Cruciate Ligament (ACL) Revision Surgery: French National Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient with an anterior cruciate ligament (ACL) revision, defined as all surgical procedures replacing the ACL graft with a new graft
- Age 18 years or older
You will not qualify if you...
- Multi-ligament injuries
- Any procedure where the ACL was not revised and an additional graft was inserted
- Patients who had already undergone their first ACL revision procedure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - From surgery to 2 months
Participants undergo ACL revision surgery and are monitored for surgical complications.
Approximately 2 post-operative visits
Duration - 24 months
Participants complete functional score questionnaires and clinical data are collected from medical records to assess recovery and outcomes.
4 visits at months 0, 6, 12, and 24
Trial Site Locations
Total: 1 location
1
CHU Saint-Etienne
Saint-Etienne, France
Actively Recruiting
Research Team
T
Thomas NERI, MD PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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