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A Clinical Trial Evaluating a Total Disc Replacement in Patients With Cervical Disc Disease — CerPass  

Cervical Disc Disease Clinical Trial

Official title:
A Prospective Observational Study Evaluating the Performance of the CerPass® Total Disc Replacement in Patients With Single-Level Cervical Disc Disease

Clinical Trial Summary

This study will be a non-randomized trial consisting of patients with single level (C3 to C7) symptomatic cervical disc disease who have not previously received fusion surgery at the same level, and have failed to improve with conservative treatment for at least 6 weeks prior to enrollment, or who present with progressive neurological symptoms or signs in the face of conservative treatment.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01433367
Study type Observational
Source NuVasive
Contact
Status Terminated
Phase N/A
Start date May 2010
Completion date December 2013
View Details
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