This study is seeking patients with degenerative cervical radiculopathy requiring surgical intervention, confirmed clinically and radiographically, at two contiguous vertebral levels from C3 to C7.
The primary objective of the study is to evaluate the safety and effectiveness of the Orthofix M6-C™ artificial cervical disc in patients with contiguous two-level symptomatic cervical radiculopathy with or without cord compression.
You may be eligible if you:
- Have been told that you need cervical spine (neck) surgery at 2 consecutive levels.
- Are between ages 18-75
- Are experiencing continued neck and/or arm pain after 6 weeks of conservative treatment
- Have no autoimmune disorders, insulin dependent diabetes, or cancer
- BMI less than 45
Please contact research@spine.md / 310-385-7766 for more information.
You may also visit ClinicalTrials.gov (identifier NCT04982835) at [ Ссылка ]
