Efficacy Study of NuCel® in Patients Undergoing Fusion of the Lumbar Spine

Status Completed

Clinical Trial Summary

The purpose of this study is to determine whether NuCel is effective in promoting spinal fusion in degenerative disease of the lumbar spine.

Clinical Trial Description

The study is a prospective, single center clinical trial to establish the efficacy of NuCel, a minimally manipulated allograft tissue, for use in lumbar interbody and intertransverse fusion procedures. Subjects will undergo standard interbody fusion surgery as per the signed informed consent with NuCel and autograft bone. Patients will be evaluated postoperatively at 6 weeks, 3 months, 6 months, 1 year, and 2 years (if required). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02023372
Study type	Interventional
Source	NuTech Medical, Inc
Contact
Status	Completed
Phase	N/A
Start date	December 2013
Completion date	August 16, 2019

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