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Clinical Trial Summary

This is a single center, prospective, randomized controlled study. The primary objective of this study is to measure migration over two years with RSA. Patients will be randomized in two arms, receiving a Taperloc Complete Reduced Distal or a Taperloc Complete Microplasty hip stem.


Clinical Trial Description

A total of 50 patients will be enrolled into the study, randomized 1:1. All patients will receive a G7 limited hole acetabular cup with E1 liner. All potential study subjects will be required to participate in the Informed Consent process. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03409666
Study type Interventional
Source Zimmer Biomet
Contact
Status Completed
Phase N/A
Start date May 12, 2017
Completion date November 6, 2020

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