Predictive Factors of Good Results After Multiligamentar Knee Reconstruction (MLKR)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Datas collected.
- Who it may be relevant to
- Registry conditions: Knee Ligament Injury. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Multiligamentar knee injury has consequences on knee function (instability, arthritis, life disagreement). Surgical reconstructions have known recent evolutions. The goal of this study is to evaluate functional and clinical results at one year of those new surgical technics. A clinical and functional follow up will be performed before the surgery, then at 6 months and one year.
Detailed description
Patients will also benefit of a Magnetic Resonance Imaging (MRI) and isokinetic evaluations at one year.
Interventions
- Other Datas collected
Datas collected by medical record: medical data (weight, height, smoking status, history) and socio-demographic data (age, occupation, type of injury) information, assessment of knee function before surgery, at 6 months and 1 year after surgery, magnetic resonance imaging (MRI) and radiological imaging at 1 year after surgery, results of the Iso-kinetic Muscle Assessment Test at 1 year after surgery to objectively determine the recovery of muscle function The data collected will be used to perf
Primary outcome measures
- Functional score : International Knee Documentation Committee (IKDC) [Time frame: Months : 0, 6 and 12]
Secondary outcome measures (6)
- Functional score : Knee Injury and Osteoarthritis Outcome Score (KOOS) [Time frame: Months : 0, 6 and 12]
- Visual Analogue Scale (VAS) scale [Time frame: Months: 0, 6 and 12]
- Laxity [Time frame: Month : 12]
- Joint amplitudes [Time frame: Months: 0, 6 and 12]
- Clinical data [Time frame: Month : 0]
- Recovery of muscle function [Time frame: Month : 12]
Eligibility criteria
Inclusion criteria
- Any patient who benefits of a multiligamentar knee reconstruction at hospital of Saint-Etienne
Exclusion criteria
- Refusal
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
France · 1 center
- CHU Saint-Etienne — Saint-Etienne
Identifiers
NCT: NCT06024850 · IRBN342022/CHUSTE