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Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis

Spondylolisthesis Clinical Trial

Official title:
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis

Clinical Trial Summary

The purpose of this clinical investigation is to evaluate the clinical outcomes of subject with spondylolisthesis undergoing posterolateral fusion (PLF) surgery utilizing the Aspen™ Spinous Process Fixation System. The Aspen™ device will be evaluated using Oswestry Disability Index (ODI) improvement and success of fusion.

Clinical Trial Description

Evaluate the clinical outcomes of subject with spondylolisthesis undergoing posterolateral fusion (PLF) surgery utilizing the Aspen™ Spinous Process Fixation System. The Aspen™ device will be evaluated using Oswestry Disability Index (ODI) improvement and success of fusion. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01560273
Study type Observational
Source Zimmer Biomet
Contact
Status Terminated
Phase
Start date February 2012
Completion date September 2015
View Details
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