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Clinical Trial Summary

To demonstrate the safety and effectiveness of the Trinity™ BIOLOX delta™ Ceramic-on-Ceramic Total Hip System in comparison to the Trinity™ Acetabular Hip System,which is FDA cleared for use in the U.S. The comparison will be based upon clinical success at the Month 24 endpoint.


Clinical Trial Description

The clinical research results for the Trinity™ BIOLOX delta™ Ceramic-on-Ceramic Total Hip System will be compared to the control device Clinical success is based upon Harris Hip Scores to evaluate functional status, adverse events, radiological assessments and no device failure (defined as removal, replacement, or modification of any device component). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01921309
Study type Interventional
Source Corin
Contact
Status Active, not recruiting
Phase N/A
Start date December 2012
Completion date December 2021

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