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Postmarket Outcomes Study for Evaluation of the Superion™ Spacer — PRESS2  

Lumbar Spinal Stenosis Clinical Trial

Official title:
Postmarket Outcomes Study for Evaluation of the Superion™ Spacer

Clinical Trial Summary

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

Clinical Trial Description

The purpose of this outcomes study is to compile real-world outcomes for the commercially approved Indirect Decompression Systems (IDS) in routine clinical practice when used according to the applicable Instructions for Use. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04563793
Study type Observational
Source Boston Scientific Corporation
Contact
Status Completed
Phase
Start date October 8, 2020
Completion date March 20, 2023
View Details
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