Clinical Trial

Retrospective Analysis of Patients Implanted With 2 Levels of Prodisc® C Vivo Devices

Enrolling by Invitation
View on ClinicalTrials.gov →
Summary
The objective of the study is to evaluate the safety and post-operative performance profile of the prodisc® C Vivo after implantation in comparison to the relevant clinical literature.
Trial Details
NCT Number NCT07370493
Lead Sponsor Centinel Spine
Collaborators: Avania
Conditions Degenerative Disc Disease, Cervical Spine Degenerative Disease, Symptomatic Cervical Disc Disease, Cervical Spine Degenerative Disc Disease
Enrollment 200 participants
Start Date 2025-11-01
Primary Completion 2030-12 (estimated)
Study Completion 2030-12 (estimated)
Updated on ClinicalTrials.gov 2026-01-27