Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05883436

Investigation of DEXA-C Anterior Cervical Interbody System

Led by Aurora Spine and Pain · Updated on 2025-10-02

80

Participants Needed

4

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Investigation of DEXA-C Anterior Cervical Interbody System

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Scheduled or planned for anterior cervical discectomy and fusion using the DEXA-C system at levels C3 to C7 with supplemental fixation and/or allogenic bone graft
  • Radicular signs and symptoms in one or both arms such as pain, numbness, or weakness affecting a nerve root
  • Diagnosis of cervical radiculopathy at one or two contiguous levels from C3 to C7 needing open anterior cervical fusion and discectomy
  • Diagnosis of degenerative disc disease confirmed by imaging showing disc herniation or osteophytes with clinical symptoms
  • At least 6 weeks of prior conservative treatment like physical therapy or pain medication
Not Eligible

You will not qualify if you...

  • History of cervical spine surgery within 12 months before this surgery
  • Diagnosis of severe spondylosis
  • Need for posterior cervical surgery, anterior cervical corpectomy, or revision surgery
  • Membership in a vulnerable population such as minors, adults unable to consent, or pregnant women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

UCI Center for Clinical Research

Orange, California, United States, 92868

Actively Recruiting

2

Orthopaedic Institute of Western KY

Paducah, Kentucky, United States, 42003

Actively Recruiting

3

Koga Neurosurgery

Covington, Louisiana, United States, 70433

Actively Recruiting

4

Optima Orthopedics

Oklahoma City, Oklahoma, United States, 73159

Actively Recruiting

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Research Team

S

Sarah Martineck, PA

CONTACT

M

Matthew Goldstone

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

1

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