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Clinical Trial Summary

This trial studies the side effects of OsteoCrete in filling bone voids in participants with bone voids or defects. OsteoCrete may eliminate the need for further surgery and the removal of healthy bone.


Clinical Trial Description

PRIMARY OBJECTIVES: I. To assess the safety of the device, which for the purpose of this study is defined as the compound injected into bone. SECONDARY OBJECTIVES: I. To determine the rate of absorption and bone ingrowth. OUTLINE: Participants receive OsteoCrete intraoperatively to fill voids that occur in bones during surgery or to augment screw fixation. After completion of study treatment, participants are followed for up to 1 year. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04069923
Study type Interventional
Source Jonsson Comprehensive Cancer Center
Contact
Status Completed
Phase N/A
Start date December 18, 2018
Completion date January 17, 2022

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