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Recruiting NCT05876143

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

Conditions: Unicompartmental Knee Arthroplasty

Sponsor: Societe dEtude, de Recherche et de Fabrication

trial.available_in: БГ
Overview
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
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.
Interventions
Unicompartmental knee arthroplasty
DEVICE
Locations 1
France (1)
CHU Lyon Sud
Pierre-Bénite
Technical details
Status
Recruiting
Study type
OBSERVATIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
01.01.2023
Completion date
31.01.2035
Registry ID
NCT05876143
Source
clinicaltrials.gov
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