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Efficacy and Safety of Integra Accell Evo3 DBM in Instrumented Lumbar Spine Fusion

Stenosis Clinical Trial

Official title:
Efficacy and Safety of Integra Accell Evo3 Demineralized Bone Matrix in Instrumented 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 instrumented lumbar 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 instrumented lumbar spine fusion in comparison to a retrospective cohort of Infuse subjects. Infuse subjects were not enrolled in the current study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01714804
Study type Interventional
Source SeaSpine, Inc.
Contact
Status Completed
Phase N/A
Start date August 2012
Completion date October 2016
View Details
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