Clinical Evaluation of GENEX® DS in Instrumented Posterolateral Fusion

Status Terminated

Clinical Trial Summary

The overall goal of this clinical study is to characterize the fusion rate of geneX® ds bone graft substitute in comparison to autograft, which is considered the gold standard for posterolateral fusion. Assessments are made using AP and Lateral x-rays, F/E x-rays, and CT scans geneX® ds has been cleared by the FDA for use in these procedures; however this study will allow more detailed characterization of geneX® ds performance in the long-term (1 year). By using the patient as their own control, direct comparison to autograft can be performed while minimizing other variables.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02317185
Study type	Observational
Source	Spine Wave
Contact
Status	Terminated
Phase
Start date	December 2014
Completion date	December 2016

View Details

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