Investigation of DEXA-C Anterior Cervical Interbody System

Recruiting now · Not applicable

Conditions studied: Degenerative Disc Disease

In brief

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

Key facts

Study ID

NCT05883436

Run by

Aurora Spine and Pain

People needed

80

Starts

2023-02-22

Expected to finish

2027-02-22

Last updated by the study team

2025-10-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Must already be scheduled or planned for anterior cervical discectomy and fusion using the Dexa-C Anterior Interbody System C3-7 with supplemental fixation and/or allogenic bone graft composed of cancellous, cortical, and/or cortico-cancellous bone meeting on-label criteria.
• Radicular signs and symptoms in one or both arms (i.e., pain, paresthesia or paresis in a specific nerve root distribution).
• Diagnosis of cervical radiculopathy at one or two contiguous levels from C3-7 requiring open anterior cervical fusion and discectomy.
• Diagnosis of degenerative disc disease by radiographic evidence of cervical disc herniation and/or osteophytes accompanying clinical symptoms.
• At least 6 weeks prior conservative treatment (i.e. physical therapy, pain medication).

You may not qualify if…

• History of cervical spine surgery less than 12 months prior to surgery.
• Diagnosis of severe spondylosis.
• Patients requiring posterior cervical surgery, anterior cervical corpectomy, or revision surgery.
• Any member of a vulnerable population (ie. minors, adults who lack the ability to consent, pregnant women, etc.)

Where it is running

• UCI Center for Clinical Research — Orange, California, United States (enrolling)
• Orthopaedic Institute of Western KY — Paducah, Kentucky, United States (enrolling)
• Koga Neurosurgery — Covington, Louisiana, United States (enrolling)
• Optima Orthopedics — Oklahoma City, Oklahoma, United States (enrolling)

Full record on ClinicalTrials.gov

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