Postmarket Outcomes Study for Evaluation of the Superion™ Spacer
NCT04563793 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 129
Last updated 2025-01-13
Summary
To compile real-world outcomes of the Superion™ IDS in routine clinical practice.
Conditions
- Lumbar Spinal Stenosis
Interventions
- DEVICE
-
Superion™ IDS
All patients to receive IDS for the treatment of moderate Lumbar Spinal Stenosis symptoms.
Sponsors & Collaborators
-
Boston Scientific Corporation
lead INDUSTRY
Principal Investigators
-
Natalie Bloom Lyons · Boston Scientific Corporation
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-10-08
- Primary Completion
- 2023-03-20
- Completion
- 2023-03-20
- FDA Device
- Yes
Countries
- United States
Study Locations
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