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Clinical Trials in France / NCT05323474
Recruiting Not applicable

Optimized Rehabilitation After Anterior Cruciate Ligament Before Returning to Sport

NCT05323474 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2022-11-14
Last updated
2026-04-24

Condition(s) studied

Ligament Knee InjuryAnterior Cruciate Ligament Rupture

Investigational drug(s) / intervention(s)

Usual rehabilitationRehabilitation optimized

Usual rehabilitation: Usual rehabilitation according to the practice of the "Haute Autorité de Santé" (HAS)

Rehabilitation optimized: Rehabilitation optimized according to the study protocol

Study summary

Following reconstruction of the anterior cruciate ligament (ACL), a standardized rehabilitation protocol is carried out by a physiotherapist. In France, a well-established rehabilitation consensus guides the first phase of 3 months postoperatively and patient compliance is generally excellent. The next phase should allow a return to sport (RTS) following a continuum depending on the objectives of the sport's patient, starting with a return to running activities (RTR) and a preparatory phase for a RTS which may be authorized at 6 months post-op.

This multicentre randomized control trial aims to evaluate the effectiveness of an individualized and optimized rehabilitation program guided by monthly assessments carried out by physiotherapists from the 3rd to the 6th month postoperatively to reduce the risk of new ACL injuries (operated or healthy knee), compared to standard management.

Eligibility

Sex
ALL
Min age
18 Years
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria: * Affiliation to the French Social Security system * Patient who has had an ACL reconstruction regardless of the standard surgical technique used * Patient with a sports activity, pivot and/or contact (e.g. soccer, basketball, handball, rugby, judo...) and practiced in competition (Tegner sports activity scores \>7 and Marx scores \>11 before the accident. * Patient wishing to return to competitive sport * Consent signed by the patient Exclusion Criteria: * Contralateral or bilateral involvement or operated on for a re-injury of the ACL * Patients with a medical contraindication to the performance of one of the tests * Patients suffering from a neurological (motor and/or sensitive), vestibular or rheumatic pathology * Patient performing rehabilitation with a physiotherapist who does not wish to participate in the study. * Pregnant or breastfeeding woman * Patient under guardianship or curators

Primary outcome measure(s)

Trial sites (8)

FacilityCityRegionStatus
Medipole de Savoie Challes-les-Eaux France Recruiting
Clinique de Domont Ortholab Domont France Not Yet Recruiting
Centre Hospitalier de Firminy Firminy France Not Yet Recruiting
Clinique de La Sauvegarde Lyon France Recruiting
Hopital de La Croix Rousse Lyon France Not Yet Recruiting
Hôpital Lyon Sud Lyon France Not Yet Recruiting
CHU de Saint-Etienne Saint-Etienne France Recruiting
Hôpital de la Tour Geneva Switzerland Not Yet Recruiting

More Centre Hospitalier Universitaire de Saint Etienne trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05323474 on ClinicalTrials.gov ↗ ← All trials in France