๐๏ธ Verified NIH Record โข Updated 2026-08-21
Investigation of DEXA-C Anterior Cervical Interbody System (NCT05883436)
A Prospective, Multi-Center Investigation of the DEXA- C Anterior Cervical Interbody System
๐ต Active, Not Recruiting Observational / Diagnostic โ๏ธ Medical Device Protocol Sponsor: Aurora Spine and Pain
๐ฉบ Plain-English Summary (8th-Grade Level)
FDA Cleared interbody product for the cervical spine, designed to match a patients DEXA scan for increase in fusion rate.
Who can join: Review the eligibility criteria below.
Location: UCI Center for Clinical Research โ Orange, California
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (4 Sites)
- UCI Center for Clinical Research โ Orange, California
- Orthopaedic Institute of Western KY โ Paducah, Kentucky
- Koga Neurosurgery โ Covington, Louisiana
- Optima Orthopedics โ Oklahoma City, Oklahoma
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.