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Clinical and Radiographic Outcomes of TLIF w/3D Printed Cellular Implant

Degenerative Disc Disease Clinical Trial

Official title:
Clinical and Radiographic Outcomes of Transforaminal Lumbar Interbody Fusion (TLIF) With a Novel 3D Printed Cellular Titanium Implant

Clinical Trial Summary

This study is designed to evaluate clinical outcomes and spine fusion rates for patients undergoing transforaminal lumbar interbody fusion using the CONDUIT 3D printed titanium TLIF cage.

Clinical Trial Description

This prospective, single-center study is being conducted as a post market evaluation of the CONDUIT 3D printed titanium TLIF Cage. Patients undergoing transforaminal lumbar interbody fusions due to lumbar spinal pathology (i.e. central foraminal stenosis, degenerative disc disease, and/or lumbar spondylolisthesis) and have failed conservative care will be recruited for this study. Patients will be serially evaluated at 6 month intervals for a total of 24 months post index procedure to assess patient reported outcomes, clinical outcomes, and radiographic parameter, specifically spine fusion rates. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05023733
Study type Observational
Source Hartford Hospital
Contact Bethany Samperi
Phone 860-972-5978
Email bethany.samperi@hhchealth.org
Status Recruiting
Phase
Start date October 1, 2021
Completion date October 1, 2025
View Details
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