Phase
Condition
N/ATreatment
total knee arthroplasty with ultra-congruent polyethylene
total knee arthroplasty with medial pivot polyethylene
Clinical Study ID
Ages 18-90 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion criteria :
Subjects 18 to 90 years of age, eligible for a primary total knee replacement for gonarthrosis
Competent subjects able to give informed consent to participate in the research
Affiliation to the social security system
Exclusion criteria :
Infection history of the knee to be replaced
Deformity greater than 15 degrees
Any surgical and/or anesthetic contraindication, or any condition deemed by the investigator to be incompatible with the research.
Any contraindication mentioned in the instructions for use of the medical device
Pregnant or breastfeeding women
Recent infection history of the surgical site
Adults who are subject to a legal protection measure or who are unable to express their constent (Article L1121-8 of the French Public Health Code) and subjects under judicial protection (article L. 1122-2 FPHC)
Subjects who refuse to participate
Study Design
Study Description
Connect with a study center
CHU de Clermont-Ferrand
Clermont-Ferrand,
FranceActive - Recruiting
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