Omnifit Hydroxylapatite (HA) Hip Outcomes Study

Status Terminated

Clinical Trial Summary

The purpose of this study was to obtain up to 25 year post-operative data on the Omnifit Hydroxylapatite (HA) Hip System in support of the hypothesis that it is a satisfactory system for reducing implant loosening, permitting tissue bonding onto the hydroxylapatite surfaces of the implant and providing a safe, efficient, and well-functioning hip in a wide spectrum of clinical circumstances.

Clinical Trial Description

n/a

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Arthroplasty, Replacement, Hip

Clinical Trial Details

NCT number	NCT00958347
Study type	Interventional
Source	Stryker Orthopaedics
Contact
Status	Terminated
Phase	N/A
Start date	October 1987
Completion date	May 2011

View Details

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