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Investigation of DEXA-C Anterior Cervical Interbody System — DEXA-C  

Degenerative Disc Disease Clinical Trial

Official title:
A Prospective, Multi-Center Investigation of the DEXA- C Anterior Cervical Interbody System

Clinical Trial Summary

FDA Cleared interbody product for the cervical spine, designed to match a patients DEXA scan for increase in fusion rate.

Clinical Trial Description

The DEXA-C Cervical Interbody System is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one or two contiguous levels from C2-T1. Device system is designed for use with supplemental fixation and autograft and/or allogenic bone graft composed of cancellous, cortical, and/or cortico-cancellous bone to facilitate fusion and is to be implanted via an open, anterior approach. The Dexa-C clinical study will collect data on those patients who have been treated with Dexa-C Anterior Cervical Interbody System to allow for a better understanding of outcomes associated with it. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05883436
Study type Interventional
Source Aurora Spine and Pain
Contact Kristina R Ramey, M-PH
Phone 2703664534
Email kramey@auroraspine.us
Status Recruiting
Phase N/A
Start date February 22, 2023
Completion date December 31, 2025
View Details
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