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Clinical Trials in France / NCT07489963
Recruiting Not applicable

Functional Impact at 12 Months Post-op of Posterior Cruciate Ligament Conservation During Robotic-assisted Surgery (MAKO) for Total Knee Replacement.

NCT07489963 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-10-10
Last updated
2026-03-27

Condition(s) studied

Knee Arthroplasty, Total

Investigational drug(s) / intervention(s)

Total knee arthroplasty

Total knee arthroplasty: Robot-assisted total knee arthroplasty

Study summary

Studies have been made on the best way to do knee surgery and whether to conserve the posterior cruciate ligament or not during total knee prosthesis insertion is still under debate. However, most of these studies were made before the introduction of robotic knee surgery. It seems timely to do a study comparing these two surgical techniques: preservation versus removal of the posterior cruciate ligament in knee arthroplasty

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient scheduled for first-intention robotic-assisted total knee replacement (MAKO). * Unilateral replacement, regardless of laterality. * Patient able to answer questionnaires. * Patient willing to undergo usual 12-month follow-up. * Patient has given free and informed consent and has signed the consent form. * Patient affiliated with or benefiting from a health insurance scheme. Exclusion Criteria: * Patient with intraoperative technical impossibility of retaining PCL (flessum \> 20°, flexion stiffening \< 100°). * Previous posterior cruciate ligament surgery. * Post-traumatic gonarthrosis. * Valgus \> 185°. * Patient with septic complication. * Patient participating in another interventional trial. * Patient in an exclusion period determined by another study. * Patient under court protection, guardianship or curatorship. * Patient unable to give consent. * Patients for whom it is impossible to provide informed information. * Pregnant women

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
Clinique Tivoli-Ducos Bordeaux France Recruiting
Hôpital Croix Rousse Lyon France Recruiting
Nîmes University Hospital Nîmes France Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07489963 on ClinicalTrials.gov ↗ ← All trials in France