Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06099600

Anterior Cruciate Ligament Reconstruction

Led by GCS Ramsay Santé pour l'Enseignement et la Recherche · Updated on 2025-07-01

84

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

Sponsors

G

GCS Ramsay Santé pour l'Enseignement et la Recherche

Lead Sponsor

E

Euraxi Pharma

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study evaluates the effectiveness of a pre-habilitation stay via digital monitoring on patients' short-term post-operative anxiety, compared with conventional management.

CONDITIONS

Official Title

Anterior Cruciate Ligament Reconstruction

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18
  • Partial or complete primary anterior cruciate ligament rupture
  • Scheduled anterior cruciate ligament reconstructive surgery
  • Patient has a tablet, computer, or smartphone with an internet connection
  • Patient can understand and read French
  • Willingness to complete questionnaires at regular intervals
  • Membership of a social security scheme
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Recurrence or contralateral lesion
  • Stage III collateral ligament injury
  • Osteotomy
  • Neurological (motor and/or sensory), vestibular, or rheumatic pathology
  • Pregnant or breast-feeding woman
  • Protected adult patient (under guardianship, curatorship, or deprivation of liberty)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Clinique de la Sauvegarde

Lyon, France, 69009

Actively Recruiting

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Research Team

D

David DEJOUR, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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