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Cormet Post-PMA Study: New Enrollment — PASNew  

Rheumatoid Arthritis Clinical Trial

Official title:
Cormet Hip Resurfacing System Post-PMA Study Group (New Enrollment)

Clinical Trial Summary

The primary objective of this study is to evaluate the performance of the Cormet Hip Resurfacing implant system in the post-approval environment.

Clinical Trial Description

This study tracks the performance of the Cormet Hip Resurfacing system in the post-approval environment to see if there are significant changes in device performance from the pre-market IDE setting as compared to the post-approval setting. Specifically this study will compare the proportion of subjects achieving a Month 24 composite clinical success (CCS) criterion and 24 month cumulative revision rate among the newly enrolled post-approval study subjects to the IDE subjects' performance on CCS as reported in the Pre-Market Application (PMA). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00722007
Study type Interventional
Source Corin
Contact
Status Completed
Phase N/A
Start date April 24, 2008
Completion date May 12, 2014
View Details
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