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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


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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