Brief Title
Risk of Osteoarthritis of the Knee at Least 5 Years After ACL Reconstruction: Comparative Study Between an Isolated ACL Reconstruction and a Reconstruction Combining ACL and ALL
Official Title
Risk of Osteoarthritis of the Knee at Least 5 Years After ACL Reconstruction: Comparative Study Between an Isolated ACL Reconstruction and a Reconstruction Combining ACL and ALL
Brief Summary
The main objective of this study is to compare, with a minimum follow-up of 5 years, the prevalence of femoro-tibial osteoarthritis after an isolated ACL ligamentoplasty or after an ACL ligamentoplasty combining ACL and ALL.
Study Type
Interventional
Primary Outcome
Assessment of the prevalence of femoro-tibial osteoarthritis
Condition
ACL
Intervention
Radiography
Study Arms / Comparison Groups
Patient operated with isolated ACL knee reconstruction
Description:
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Recruitment Status
Procedure
Estimated Enrollment
180
Start Date
April 15, 2020
Completion Date
December 15, 2021
Primary Completion Date
April 15, 2021
Eligibility Criteria
Inclusion Criteria: - Patients who underwent an isolated Anterior Cruciate Ligament (ACL) reconstruction or a combined ACL and anterolateral ligament reconstruction (Extra Articular Plasty) between January 1, 2011 and March 31, 2012. - Patients affiliated or beneficiaries of a social security scheme - Patients who have given their express consent. Exclusion Criteria: - Patients with pediatric ACL reconstruction technique - Patients with a complex associated gesture such as osteotomy or ligamentoplasty other than extra articular plastic surgery. - Contraindication to a radio control (pregnancy) - Patient's refusal to participate in the study - Protected patients: Adults under guardianship, curatorship or other legal protection, deprived of their liberty by judicial or administrative decision; Pregnant, breastfeeding or parturient woman; Hospitalized without consent.
Gender
All
Ages
18 Years - N/A
Accepts Healthy Volunteers
No
Contacts
, 0683346567, [email protected]
Location Countries
France
Location Countries
France
Administrative Informations
NCT ID
NCT05123456
Organization ID
2018-A02447-48
Responsible Party
Sponsor
Study Sponsor
Ramsay Générale de Santé
Collaborators
European Clinical Trial Experts Network
Study Sponsor
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Verification Date
November 2021