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

ENROLLING BY INVITATION

NCT07370493

Sponsor: Centinel Spine

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.

Official title: A Multicenter, Retrospective Analysis to Evaluate Radiographic Outcomes and Safety Profiles Along Prospective Follow-Up Periods for Patients Implanted With 2 Levels of Prodisc® C Vivo Devices.

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

200

Start Date

2025-11-01

Completion Date

2030-12

Last Updated

2026-01-27

Healthy Volunteers

No

Conditions

Degenerative Disc Disease Cervical Spine Degenerative Disease Symptomatic Cervical Disc Disease Cervical Spine Degenerative Disc Disease

Interventions

DEVICE

Prodisc C Vivo

The prodisc® C Vivo device is a non-keeled cervical disc replacement prosthesis. The device is modular intervertebral disc prostheses designed to replace a diseased and/or a degenerated disc of the cervical spine in SCDD patients, thereby restoring disc height, biomechanical stability and allowing the potential for motion at the affected vertebral segment.

Locations (1)

ONZ Spine

Recklinghausen, Germany

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