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Clinical Trial Comparing Decompression With and Without Coflex™ Interlaminar Technology Treating Lumbar Spinal Stenosis

Spinal Stenosis Clinical Trial

Official title:
Comparative Evaluation of Clinical Outcome in the Treatment of Degenerative Spinal Stenosis With Concomitant Low Back Pain by Decompression With and Without Additional Stabilization Using the Coflex™ Interlaminar Technology

Clinical Trial Summary

A 2 year comparative evaluation of clinical outcome in the treatment of degenerative spinal stenosis with concomitant low back pain by decompression with and without additional stabilization using the coflex® Interlaminar Technology

Clinical Trial Description

The coflex® implant for interlaminar stabilization has been in clinical use for more than 10 years and is CE-certified according to the standards and approved in the United States.

This was a randomized multicenter study to collect prospective data for potential improvement in the therapy of low back pain during the treatment of spinal stenosis. The study was conducted in Germany. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01316211
Study type Interventional
Source Paradigm Spine
Contact
Status Completed
Phase N/A
Start date January 2008
Completion date August 2014
View Details
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