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Open Label Study to Collect Clinical Data to Document Clinical Performance and Safety in Total Knee Arthroplasty

Total Knee Arthroplasty Clinical Trial

Official title:
A Prospective and Retrospective, Open Label Study to Collect Clinical Data to Document Clinical Performance and Safety in Total Knee Arthroplasty Using HLS Implants

Clinical Trial Summary

The purpose of this study is to evaluate clinical performance and safety in total knee arthroplasty using HLS implants.

Clinical Trial Description

It is planned to collect prospective and retrospective data from a continuous and exhaustive series of patients in a French center where Total Knee Arthroplasty with HLS prosthesis is performed routinely. All patients treated with HLS KneeTec (cemented, non-cemented or hybrid versions) implant will be included. All eligible patients seen in consultation and who agree to participate in the study should be included, systematically and consecutively, since the initiation of the study. Data will be collected retrospectively for HLS I, II, Evolution and Noetos® implants, and when prospectively for cementless, cemented and hybrid HLS KneeTec prosthesis. Post-surgery visit data will be collected at 1-y , 3-y , 5-y, 10-y FU visits per protocol then up to the latest FU visit available. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04727060
Study type Observational
Source Corin
Contact Vanessa GRIMAUD
Phone 0667267075
Email vanessa.grimaud@coringroup.com
Status Recruiting
Phase
Start date December 15, 2011
Completion date June 2031
View Details
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