Ambispective Open Multicentric Study Evaluating Clinical Results of Unicondylar Knee Arthroplasty Performed With U-Knee/Uni-Kroma Implants
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• \- All patients using a U-Knee / Uni-Kroma unicompartmental knee prosthesis and benefiting from the social security affiliation scheme.
Locations
Other Locations
France
CHU Lyon Sud
RECRUITING
Pierre-bénite
Contact Information
Primary
Clinical Department
clinical@serf.fr
0472056010
Time Frame
Start Date: 2023-01-01
Estimated Completion Date: 2035-01-31
Participants
Target number of participants: 400
Treatments
Fixed cementless UKP
Patient implanted with a fixed cementless Unicompartmental prosthesis
Fixed cemented UKP
Patient implanted with a fixed cemented Unicompartmental prosthesis
Mobile Cementless UKP
Patient implanted with a mobile cementless Unicompartmental prosthesis
Mobile Cemented UKP
Patient implanted with a mobile cemented Unicompartmental prosthesis
Fixed Cementless UKP (TIT coating)
Patient implanted with a fixed cementless Unicompartmental prosthesis coating with TIT
Related Therapeutic Areas
Sponsors
Leads: Societe dEtude, de Recherche et de Fabrication