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

Enrolling by invitation

Conditions studied: Degenerative Disc Disease, Cervical Spine Degenerative Disease, Symptomatic Cervical Disc Disease, Cervical Spine Degenerative Disc Disease

In brief

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.

Key facts

Study ID

NCT07370493

Run by

Centinel Spine

People needed

200

Starts

2025-11-01

Expected to finish

2030-12-01

Last updated by the study team

2026-01-27

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• In order for a patient's data to be included in this study, he/she has to meet the indications and not possess any of the specific or general contraindications listed in the Instructions For Use (IFU).
• They must provide written informed consent with appropriate documentation noted in source documentation (prospective cohort only).

You may not qualify if…

• There are no additional exclusion criteria.

Where it is running

• ONZ Spine — Recklinghausen, Germany

Full record on ClinicalTrials.gov

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