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 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 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

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

, , 

Verification Date

November 2021