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Clinical Trial Summary

This study compares the fill of bone graft sites in the knee. It is hypothesized that harvest sites, voids, and defects caused by trauma that are treated with the OsseoFit™ Porous Tissue Matrix™ device will achieve a better fill grade than those treated with the conventional method.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00708474
Study type Interventional
Source Zimmer Biomet
Contact
Status Withdrawn
Phase N/A
Start date June 2008
Completion date February 2009

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