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Efficacy and Safety of Accell Evo3 Demineralized Bone Matrix (DBM) in Instrumented Posterolateral Lumbar Spine Fusion

Stenosis Clinical Trial

Official title:
Efficacy and Safety of Integra Accell Evo3 Demineralized Bone Matrix Instrumented Posterolateral Lumbar Spine Fusion

Clinical Trial Summary

The objective of this study is to prospectively evaluate the performance of Integra Accell Evo3 Demineralized Bone Matrix as an adjunct for posterolateral spine fusion with a retrospective comparison to a historical patient cohort.

Clinical Trial Description

The objective of this study is to prospectively evaluate the performance of Integra Accell Evo3 Demineralized Bone Matrix as an adjunct for posterolateral spine fusion with a retrospective comparison to a historical patient cohort. The historical patient cohort has not been previously published and therefore, no reference to this group can be provided. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01430299
Study type Interventional
Source SeaSpine, Inc.
Contact
Status Completed
Phase N/A
Start date June 2011
Completion date October 2016
View Details
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