Continuum™ Metal Bearing System in Total Hip Arthroplasty

Status Completed

Clinical Trial Summary

The study is a multi-center, prospective, non-controlled, consecutive cohort post market surveillance study. The objective of this study is to obtain survival and outcome data on the Continuum Metal Bearing System in primary total hip arthroplasty.

Clinical Trial Description

The subject of this clinical investigation is the Continuum Metal Bearing THA System in primary total hip arthroplasty. This system consists of a cementless modular Trabecular Metal™ (TM) Continuum Acetabular Shell, a modular Metasul Taper liner, and a modular Metasul femoral head. The characteristics of this THA system may allow for reduction in wear and osteolysis as compared to other approved and marketed THA systems and thus increase the expected implant life. In total, 3 centers will be involved. This number of clinical sites will permit assessment of the consistency among a multitude of investigators. A total number of 100 subjects will be included in the study. It is anticipated that each clinical site will enroll 10 to 45 eligible study subjects, who have provided written informed consent. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03382652
Study type	Observational
Source	Zimmer Biomet
Contact
Status	Completed
Phase
Start date	February 9, 2011
Completion date	October 22, 2022

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