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Evaluation of Vitoss With and Without BMA for Benign Cavitary Lesions

Bone Diseases Clinical Trial

Official title:
A Combined Retrospective and Prospective Protocol to Evaluate Vitoss With and Without Bone Marrow Aspirate for Benign Cavitary Lesions

Clinical Trial Summary

This is a retrospective, two-arm study reviewing the healing of cavitary defects in patients treated with Vitoss alone versus those treated with Vitoss with bone marrow aspirate (BMA). There will be a prospective follow-up visit at 24+ months to evaluate lont-term healing in patients identified during the retrospective portion of the study. It is thought that the inclusion of BMA will facilitate the resorption of the graft material, leading to better long-term bone healing.

Clinical Trial Description

n/a

Study Design

Observational Model: Case Control

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02165943
Study type Observational
Source Orthovita d/b/a Stryker
Contact
Status Enrolling by invitation
Phase N/A
Start date January 2014
Completion date December 2014
View Details
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