PMCF Study of MPS-Flex® Knee System in TKA

Status Recruiting

Clinical Trial Summary

The objective of this study is to obtain implant survivorship and clinical outcomes data for the commercially available MPS-Flex® Total Knee Joint Prostheses used in primary total knee arthroplasty (TKA).

Clinical Trial Description

This is a retrospective and prospective, multi-centre, post-market clinical follow-up study involving orthopedic surgeons skilled in TKA and experienced implanting the devices included in this study. Patient demographic and operative information will be collected retrospectively. Postoperative clinical outcome, radiographic assessment and adverse events will be collected prospectively starting from the first year of postoperative follow up visit. All study subjects have undergone routine preoperative clinical evaluations prior to their THA, and implanted MPS-Flex® Total Knee Joint Prostheses in accordance to indications and intended use, and appropriate surgical technique(s) will be invited to participate in the study at their first year of postoperative follow up visit, and sign ICF. ;

Study Design

Related Conditions & MeSH terms

Total Knee Arthroplasty

Clinical Trial Details

NCT number	NCT04427722
Study type	Observational
Source	Zimmer Biomet
Contact	Lydia Wang
Phone	86-21-2220
Email	lydia.wang@zimmerbiomet.com
Status	Recruiting
Phase
Start date	February 25, 2021
Completion date	December 31, 2032

View Details

See also
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