RecruitingNCT04460989
Assessment of Patient Satisfaction After Arthroplasty: A Comparative Study by Implant Type
Evaluation of the Impact of Customization of Total Knee Prostheses on Patient Satisfaction and Functional Outcome of Arthroplasty.
Sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
Enrollment
480 participants
Start Date
Oct 27, 2021
Study Type
OBSERVATIONAL
Conditions
Summary
The main objective of this study is to evaluate the benefit of personalized prostheses compared to conventional prostheses on patient satisfaction 24 months after total knee arthroplasty.
Eligibility
Min Age: 18 Years
Inclusion Criteria3
- Adult man or woman who has signed consent to participate in the study
- Patient with uni- or bilateral primary gonarthrosis
- For which an indication for total knee arthroplasty has been established
Exclusion Criteria11
- History of knee arthroplasty or osteotomy
- History of knee fracture
- Inflammatory rheumatic disease or any other progressive concomitant disease that may affect the patient's functional prognosis.
- Joint or extra-articular deformities of the lower limb of traumatic origin
- Neurological diseases, stroke sequelae
- Mental disability or any other reason that may hinder the understanding or strict application of the protocol
- Patient not affiliated to the French social security scheme
- Patient under legal protection, guardianship or trusteeship
- Patient already included in another therapeutic study protocol or having participated in another trial within the previous three months
- Arthroplasty actually performed
- Absence of per operative complications in bone (femoral or tibial bone), ligament (rupture or disinsertion of the patellar or quadricipital tendon) or nerve (lesion of the external popliteal sciatica).
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Interventions
PROCEDUREarthroplasty
total knee replacement
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT04460989
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