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Outcome Study of Patients Treated With Translational Cervical Plate Used to Treat Degenerative Disc Disease

Degenerative Disc Disease Clinical Trial

Official title:
Prospective Multi-Center Clinical Study of Patients With Degenerative Disc Disease Treated With Anterior Cervical Decompression and Fusion Using the Vectra-T Translational Cervical Plate.

Clinical Trial Summary

The purpose of this study is to measure the benefits of anterior (from the front) cervical (neck) surgery for degenerative disc disease. The research part of this study is the answering of questionnaires by the patient concerning their quality of life, prior to, and after surgery.

Clinical Trial Description

This is a prospective, multi-center, four-arm study designed to evaluate the clinical and radiographic outcomes in patients diagnosed with cervical degenerative disc disease (DDD) and treated using the Vectra-T Cervical Plate and the Advanced ACF or CorticoCancellous Allograft Spacer made by Synthes Spine Company (Paoli, PA). This is not an investigational study (IDE) and no investigational or experimental devices or procedures are included in this study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00443547
Study type Observational
Source Synthes USA HQ, Inc.
Contact
Status Completed
Phase
Start date March 1, 2006
Completion date April 1, 2011
View Details
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