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rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study — CRM  

Degenerative Disc Disease Clinical Trial

Official title:
A Prospective, Randomized Clinical Investigation of rhBMP-2 and Compression Resistant Matrix With the CD HORIZON® Spinal System for Posterolateral Lumbar Fusion in Patients With Symptomatic Degenerative Disc Disease

Clinical Trial Summary

The purpose of this study was to evaluate the rhBMP-2/CRM/CD HORIZON® Spinal System as a method of facilitating spinal fusion in patients with degenerative disc disease.

Clinical Trial Description

This clinical trial was conducted to evaluate the rhBMP-2/CRM/CD HORIZON® Spinal System for posterolateral fusion treatment of patients with symptomatic degenerative disc disease versus the control group of autogenous bone with the CD HORIZON® Spinal System. The investigational treatment was the open bilateral posterolateral implantation of the rhBMP-2/CRM/CD HORIZON® Spinal System. One investigational implant was placed across two adjacent transverse processes on each side of the spine during the spinal fusion procedure. The control treatment was the bilateral posterolateral implantation of the autogenous bone harvested from the iliac crest with the CD HORIZON® Spinal System. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00707265
Study type Interventional
Source Medtronic Spinal and Biologics
Contact
Status Completed
Phase Phase 3
Start date March 2002
Completion date February 2010
View Details
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