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Clinical Trial Summary

The purpose of this study is to compare outcomes of patients with degenerative disc disease undergo lumbar spinal fusion with Stryker's Tritanium® Posterior Lumbar Cage or the UniLIF PEEK implant.


Clinical Trial Description

This study protocol intends to examine the difference in efficacy between the Tritanium Posterior Lumbar Cage and the UniLIF PEEK implant with respect to how long it takes to achieve fusion of the spine. Study participants will undergo a transforaminal lumbar interbody fusion (TLIF) surgery and return for CT and x-ray follow-up to measure the degree to which fusion has been achieved. Survey methodology to assess perceived pain, level of disability, and quality of life will also be used to measure the differences between groups on these components. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03817606
Study type Interventional
Source Riverside Medical Center
Contact
Status Terminated
Phase N/A
Start date March 1, 2019
Completion date April 27, 2021

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