Evaluating outcomes after knee ligament reconstruction
Predictive Factors of Good Results After Multiligamentar Knee Reconstruction (MLKR)
This study is testing how well people recover after knee ligament surgery by checking their knee function and health before and after the operation.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 80 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier Universitaire de Saint Etienne Academic / other |
| Locations | 1 site (Saint-Etienne) |
| Trial ID | NCT06024850 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the functional and clinical outcomes of patients undergoing multiligamentar knee reconstruction at the Centre Hospitalier Universitaire de Saint Etienne. Participants will be evaluated before surgery, and then again at 6 months and one year post-operation. The study will also include Magnetic Resonance Imaging (MRI) and isokinetic evaluations to gather comprehensive data on recovery and knee function. The goal is to identify predictive factors that contribute to successful surgical outcomes.
Who should consider this trial
Good fit: Ideal candidates are patients scheduled for multiligamentar knee reconstruction at the hospital of Saint-Etienne.
Not a fit: Patients who refuse to participate in the study will not benefit from the findings.
Why it matters
Potential benefit: If successful, this study could improve surgical techniques and rehabilitation strategies for patients with knee ligament injuries.
How similar studies have performed: While there have been studies on knee ligament injuries, this specific focus on multiligamentar reconstruction outcomes is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Any patient who benefits of a multiligamentar knee reconstruction at hospital of Saint-Etienne Exclusion Criteria: * Refusal
Where this trial is running
Saint-Etienne
- CHU Saint-Etienne — Saint-Etienne, France (Recruiting)
Study contacts
- Principal investigator: Thomas NERI, MD PhD — Centre Hospitalier Universitaire de Saint Etienne
- Study coordinator: Thomas NERI, MD PhD
- Email: Thomas.Neri@chu-st-etienne.fr
- Phone: (0)477127549
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.