Follow-up on ACL reconstruction outcomes
Follow-up of Anterior Cruciate Ligament Reconstruction
This study looks at how well people recover after having surgery to fix their torn ACL, to see what works best for their healing and recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier Universitaire de Saint Etienne Academic / other |
| Locations | 1 site (Saint-Etienne) |
| Trial ID | NCT04781920 on ClinicalTrials.gov |
What this trial studies
This observational study collects data from patients who have undergone Anterior Cruciate Ligament (ACL) reconstruction to evaluate the clinical, functional, and morphological results of the procedure. The aim is to understand the variability in surgical management and rehabilitation associated with ACL injuries. By analyzing these outcomes, the study seeks to improve patient management and recovery strategies following ACL reconstruction.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals who have recently undergone ACL reconstruction.
Not a fit: Patients who have not had ACL reconstruction or those with unrelated knee injuries may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance rehabilitation protocols and surgical techniques for patients recovering from ACL injuries.
How similar studies have performed: Other studies focusing on ACL reconstruction outcomes have shown success in improving patient management and rehabilitation strategies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients having undergone an Anterior Cruciate Ligament (ACL) reconstruction Exclusion Criteria: * None
Where this trial is running
Saint-Etienne
- Chu Saint-Etienne — Saint-Etienne, France (Recruiting)
Study contacts
- Principal investigator: Thomas NERI, MD — Centre Hospitalier Universitaire de Saint Etienne
- Study coordinator: Thomas NERI, MD
- Email: thomas.neri@chu-st-etienne.fr
- Phone: (0)477127849
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.