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A 5-year Superion™ IDS Clinical Outcomes Post-Approval Evaluation (SCOPE)

Lumbar Spinal Stenosis Clinical Trial

Official title:
A 5-year Superion™ IDS Clinical Outcomes Post-Approval Evaluation (SCOPE)

Clinical Trial Summary

To compile real-world outcomes of the Superion™ IDS in routine clinical practice.

Clinical Trial Description

To compile real-world outcomes of the Superion™ IDS in routine clinical practice, when used according to the applicable Directions for Use ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04192591
Study type Interventional
Source Boston Scientific Corporation
Contact Ann Yamano
Phone 855-213-9890
Email BSNClinicalTrials@bsci.com
Status Recruiting
Phase N/A
Start date January 30, 2020
Completion date May 2032
View Details
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