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Investigating Superion™ In Spinal Stenosis

Lumbar Spinal Stenosis Clinical Trial

Official title:
A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis

Clinical Trial Summary

The proposed prospective, multi-center, randomized clinical trial is designed to evaluate the safety and effectiveness of the Superion™ ISS compared to the X-STOP® IPD® device in healthy adults suffering from at least 6 months of moderate spinal stenosis symptoms who have been unresponsive to conservative care.

Clinical Trial Description

The proposed prospective, multi-center, randomized clinical trial is designed to evaluate the safety and effectiveness of the Superion™ ISS compared to the X-STOP® IPD® device in healthy adults suffering from at least 6 months of moderate spinal stenosis symptoms who have been unresponsive to conservative care. The study endpoint is the rate of overall subject success at 24 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00692276
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Completed
Phase N/A
Start date June 2008
Completion date February 2017
View Details
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