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A Study of the In-Space Device for Treatment of Moderate Spinal Stenosis — In-Space  

Spinal Stenosis Clinical Trial

Official title:
A Multi-Center Randomized Controlled Trial of the In-Space Compared to X STOP® for Treatment of Moderate Degenerative Lumbar Spinal Stenosis

Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of the In-Space compared to the X STOP Interspinous Process Distraction (IPD) device ("X STOP") for the treatment of patients experiencing intermittent neurogenic claudication secondary to moderate degenerative lumbar stenosis at one or two lumbar levels.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00697827
Study type Interventional
Source Synthes USA HQ, Inc.
Contact
Status Terminated
Phase Phase 3
Start date June 2008
Completion date June 2011
View Details
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