Actively Recruiting
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
Eligibility Criteria
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
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
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
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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