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Clinical Trial Summary

The objective of this post-approval study is to provide scientifically valid and reliable evidence that supports claims of longer term safety and effectiveness with regard to Month 120 device survivorship rates.


Clinical Trial Description

This study will evaluate the performance of CONSERVE Plus Hip Resurfacing System under actual conditions of use. Additionally, this study will evaluate the performance of the device in the post approval environment to see if there are any significant changes in device performance as compared to the pre-market IDE Study ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Other and Unspecified Injury to Hip and Thigh

NCT number NCT01367899
Study type Observational
Source MicroPort Orthopedics Inc.
Contact
Status Terminated
Phase N/A
Start date November 2010
Completion date September 2014