Clinical trial
Investigating Superion™ In Spinal Stenosis
NCT00692276 · Boston Scientific Corporation, Industry · Completed
Key facts
| NCT number | NCT00692276 |
|---|---|
| Title | Investigating Superion™ In Spinal Stenosis |
| Official title | A Prospective, Multi-Center, Randomized Study Comparing the VertiFlex® Superion™ Interspinous Spacer (ISS) to the X-STOP® Interspinous Process Decompression (IPD®) System in Patients With Moderate Lumbar Spinal Stenosis |
| Lead sponsor | Boston Scientific Corporation, Industry |
| Collaborators | VertiFlex, Incorporated Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Lumbar Spinal Stenosis, Intermittent Claudication |
| Intervention type | Device |
| Interventions | Superion™ Interspinous Spacer, X-STOP® IPD® Device |
| Enrollment | 391 |
| Start date | Jun 1, 2008 |
| Primary completion | Feb 1, 2017 |
| Completion | Feb 1, 2017 |
| First posted | Jun 6, 2008 |
| Last update posted | Nov 16, 2020 |
| Countries | United States |
At a glance
- 10–99 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: