RecruitingNot Applicable

Ambispective Multicentric Study Evaluating UKA With U-Knee/Uni-Kroma Implants

France400 participantsStarted 2023-01-01

Plain-language summary

This clinical investigation was led as a post-market clinical follow-up study (post-market device development stage).The main objective of this study is to collect short- and medium-term clinical data on the unicondylar knee prosthesis U-Knee / Uni-Kroma, in order to evaluate the performance of these implants.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: \- All patients using a U-Knee / Uni-Kroma unicompartmental knee prosthesis and benefiting from the social security affiliation scheme. Exclusion Criteria: * Patients who objected to participating in the study and the processing of their data * Patients unable to understand the surgeon's instructions to complete their questionnaires or perform postoperative follow-up * Patients who already have a unicompartmental prosthesis on the knee in question that need to be revised.

What they're measuring

Survival rate

Timeframe: 5 years

Trial details

NCT IDNCT05876143

SponsorSociete dEtude, de Recherche et de Fabrication

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2030-01-31

Contact for this trial

Clinical Department

0472056010 clinical@serf.fr

View on ClinicalTrials.gov More Unicompartmental Knee Arthroplasty trials