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Postmarket Registry for Evaluation of the Superion® Spacer — PRESS  

Lumbar Spinal Stenosis Clinical Trial

Official title:
Postmarket Registry for Evaluation of the Superion® Spacer

Clinical Trial Summary

To gather evidence documenting the performance and clinical outcomes associated with treatment of moderate degenerative lumbar spinal stenosis using the Superion® Indirect Decompression System (IDS).

Clinical Trial Description

To gather evidence documenting the performance and clinical outcomes associated with treatment of moderate degenerative lumbar spinal stenosis using the Superion® IDS in patients ≥45 years of age suffering from symptoms of neurogenic intermittent claudication secondary to a confirmed diagnosis of moderate degenerative lumbar spinal stenosis at one or two contiguous levels from L1 to L5. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04087811
Study type Observational [Patient Registry]
Source Boston Scientific Corporation
Contact
Status Completed
Phase
Start date November 28, 2016
Completion date March 1, 2021
View Details
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