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PMCF Study on the Safety and Performance of the Alloclassic Variall Cup Ceramic Bearing System in Total Hip Arthroplasty

Osteoarthritis Clinical Trial

Official title:
Alloclassic® Variall® Cup Ceramic Bearing System in Total Hip Arthroplasty A Multi-center, Prospective, Non-controlled Post Market Surveillance Study

Clinical Trial Summary

The study is a multicenter, prospective, non-randomized, non-controlled consecutive cohort post-market clinical follow-up study.

Clinical Trial Description

The objectives of this study are to obtain survival and outcomes data on the Alloclassic® Variall® Cup in combination with the BIOLOX® delta Taper Liner and a BIOLOX® delta Femoral Head used in primary total hip arthroplasty. This will be done by analysis of standard scoring systems, radiographs and adverse event records. Two sites are involved in this study, enrolling a total of 100 patients for the study. All subjects were required to participate in the Informed Consent Process. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03672370
Study type Observational
Source Zimmer Biomet
Contact
Status Terminated
Phase
Start date March 24, 2015
Completion date May 1, 2020
View Details
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