Postmarket Registry for Evaluation of the Superion® Spacer
NCT04087811 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1674
Last updated 2023-07-06
Summary
To gather evidence documenting the performance and clinical outcomes associated with treatment of moderate degenerative lumbar spinal stenosis using the Superion® Indirect Decompression System (IDS).
Conditions
- Lumbar Spinal Stenosis
Interventions
- DEVICE
-
Superion® Indirect Decompression System (IDS)
Superion® Indirect Decompression System (IDS) (Superion® implant)
Sponsors & Collaborators
-
Boston Scientific Corporation
lead INDUSTRY
Principal Investigators
-
Natalie Bloom Lyons · Boston Scientific Corporation
Eligibility
- Min Age
- 45 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-11-28
- Primary Completion
- 2021-03-01
- Completion
- 2021-03-01
- FDA Device
- Yes
Countries
- United States
Study Locations
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