Postmarket Outcomes Study for Evaluation of the Superion™ Spacer

Completed

Conditions studied: Lumbar Spinal Stenosis

In brief

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

Key facts

Study ID
NCT04563793
Run by
Boston Scientific Corporation
People needed
129
Starts
2020-10-08
Expected to finish
2023-03-20
Last updated by the study team
2025-01-13

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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