Informing the Patient on the Type of Management, Surgical or Functional, After Rupture of the Anterior Cruciate Ligament — INFO-LCA

Ligament Rupture Clinical Trial

Official title:
Effect of Informing the Patient on the Type of Management, Surgical or Functional, After Rupture of the Anterior Cruciate Ligament : INFO-LCA

Status Recruiting

Clinical Trial Summary

The purpose of the study is to evaluate the proportion of patients after rupture of the anterior cruciate ligament (ACL) of the knee, who will have functional or surgical management (PEC) in 1st intention, after having received appropriate information.

Clinical Trial Description

As part of this study, patients will be followed for 1 year with regular functional and quality of life assessments (45 days after inclusion, 3, 6, 9 and 12 months after the start of surgical or non-surgical management). Patients who, during follow-up, will have been redirected towards surgery by the doctor (in the event of functional instability) or who will have chosen to finally move towards surgical PEC, will also be followed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05585528
Study type	Interventional
Source	GCS Ramsay Santé pour l'Enseignement et la Recherche
Contact	David DEJOUR, MD
Phone	4 72 20 00 63
Email	dejour.secretariat@lyon-ortho-clinic.com
Status	Recruiting
Phase	N/A
Start date	December 20, 2022
Completion date	March 2026

View Details

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