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Clinical Trial Summary

The aim of this study is to assess the long-term performance and safety of HLS KneeTec Deep Dish knee prosthesis when used in standard medical practice

Clinical Trial Description

It is planned to collect prospective and retrospective data from a continuous and exhaustive series of patients in a single French site where Total Knee Arthroplasty with HLS Kneetec Deep Dish prosthesis is performed routinely All patients treated with HLS KneeTec Deep Dish 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. Patients will be assessed according to the usual practice of the investigator at each participating site before surgery and then at the follow-up (FU) visits as following: 3 months (+/- 1 months); 15 months (+/- 3 months); 5 years (+/- 6 months) and 10 years (+/- 6 months). ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05211141
Study type Observational
Source Corin
Contact Vanessa GRIMAUD
Phone 0667267075
Email [email protected]
Status Recruiting
Start date February 28, 2017
Completion date November 1, 2027

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