Descriptive Study of Multiligamentary Reconstruction of the Knee
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: Clinical and radiologic evaluation.
- Who it may be relevant to
- Registry conditions: Injury, Knee. 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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Official title
Descriptive Study of Multiligamentary Reconstruction of the Knee: Clinical Results and Postoperative Laxity by Dynamic Radiography.
Overview
Evaluation of clinical results and postoperative laxity after single-stage reconstruction of multiligamentous lesions of the knee. Comparison of two types of transplant: allograft versus autograft. There is currently little data in the clinical outcome literature after allograft reconstruction. There is one study reporting postoperative laxity assessed by dynamic radiography in the four planes (anterior, posterior, varus, valgus). No study compares postoperative laxity after allograft versus autograft reconstruction.
Interventions
- Other Clinical and radiologic evaluation
Follow up post surgery: clinical and radiologic evaluation
Primary outcome measures
- Joint mobility of both knees [Time frame: 2 years]
- Postoperative laxity in varus, valgus, anterior and posterior drawer [Time frame: 2 years]
- Postoperative knee function assessed by scores [Time frame: 2 years]
Eligibility criteria
Inclusion criteria
- Patients operated for one-time allograft or autograft reconstruction of multiligamentous knee injury
- >18 years old
Exclusion criteria
- Neurological or vascular injury during trauma.
- Fracture of the femur or both bones of the leg.
- Ligamentous lesion on the contralateral knee.
- History of surgery on the affected knee.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Basic science
Study locations
France · 1 center
- CH de Versailles — Le Chesnay
Identifiers
NCT: NCT03932838 · P17/12_ Reconstruction