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Observational Study to Evaluate Clinical Performance and Safety in Total Knee Arthroplasty

Total Knee Arthroplasty Clinical Trial

Official title:
Observational Study to Evaluate the Performance and the Safety of the HLS KneeTec Cementless or Hybrid Fixations in Total Knee Arthroplasty

Clinical Trial Summary

The aim of this study is to assess the long-term performance and safety of HLS KneeTec cementless and hybrid fixation 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 French sites where Total Knee Arthroplasty with HLS Kneetec cementless and hybrid fixation knee prosthesis is performed routinely All patients treated with HLS KneeTec (cementless 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. 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: 4 months (+/- 2 months); 1 year (+/- 2 months); 5 years (+/- 12 months) and 10 years (+/- 12 months). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04872855
Study type Observational
Source Corin
Contact
Status Active, not recruiting
Phase
Start date July 17, 2020
Completion date January 15, 2032
View Details
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