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PMCF Study on the Safety and Performance of the Zimmer® Maxera™ Acetabular System in Total Hip Arthroplasty

Osteoarthritis, Hip Clinical Trial

Official title:
Zimmer® Maxera™ Acetabular System in Total Hip Arthroplasty. A Multicenter, Prospective, Non-controlled Post Market Clinical Follow-up Study

Clinical Trial Summary

This study is a multicenter, prospective, non-controlled post market clinical follow-up study. The objectives of this study are to confirm the safety and performance of the commercially available Zimmer® Maxera™ Acetabular System in Total Hip Arthroplasty.

Clinical Trial Description

The objectives of this study are to confirm the safety and performance of the Zimmer Maxera Cup mated with either a BIOLOX® delta or BIOLOX® OPTION femoral head when used in primary total hip arthroplasty. In total 250 patients will be enrolled into the study at up to 10 sites.All potential study subjects will be required to participate in the Informed Consent Process. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03372278
Study type Observational
Source Zimmer Biomet
Contact
Status Active, not recruiting
Phase
Start date January 2013
Completion date December 2028
View Details
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