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

Running, not enrolling · Not applicable

Conditions studied: Lumbar Spinal Stenosis

In brief

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

Key facts

Study ID
NCT04192591
Run by
Boston Scientific Corporation
People needed
166
Starts
2020-01-30
Expected to finish
2041-02-01
Last updated by the study team
2026-08-06

Who can join

Age: 45 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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