Restore CLINICAL TRIAL

This is a prospective, concurrently controlled, multi-center study to evaluate the safety and effectiveness of the Spinal Kinetics M6-C artificial cervical disc compared to anterior cervical discectomy and fusion (ACDF) for the treatment of symptomatic cervical radiculopathy with or without cord compression. Some participating sites will enroll just M6-C patients, while others will enroll just ACDF patients. Patients eligible for study enrollment will present with degenerative cervical radiculopathy requiring surgical intervention, confirmed clinically and radiographically, at one vertebral level from C3 to C7. A total of 243 subjects will be included at up to 20 sites.

PI: John Ratliff, MD, FACS
Trial ID: NCT01609374
Status: Recruiting

COMPaSS (Clinical Outcome Measures in Personalized aprevo Spine Surgery) Registry

PI: Atman Desai, MD
Study status: Active/Not enrolling
Research Coordinator: Banu Priya
Contact: bpriya@stanford.edu