Clinical trial
Post-Approval Study of the NexStent Carotid Stent System and the FilterWire EZ…
NCT00478673 · Boston Scientific Corporation, Industry · Terminated
Key facts
| NCT number | NCT00478673 |
|---|---|
| Title | Post-Approval Study of the NexStent Carotid Stent System and the FilterWire EZ Embolic Protection System: SONOMA |
| Official title | The NexStent® Carotid Stent System: A Post Market Approval Evaluation Study In Conjunction With the FilterWire EZ™ Embolic Protection System |
| Acronym | SONOMA |
| Lead sponsor | Boston Scientific Corporation, Industry |
| Status | Terminated |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Carotid Stenosis |
| Intervention type | Device |
| Interventions | NexStent Carotid Stent System (Monorail Delivery System), FilterWire EZ™ Embolic Protection System |
| Enrollment | 298 |
| Start date | May 1, 2007 |
| Primary completion | Jul 1, 2009 |
| Completion | Jul 1, 2009 |
| First posted | May 25, 2007 |
| Last update posted | Aug 7, 2012 |
| Countries | United States |
At a glance
- 10–99 Study sites
- Yes Results posted
- 1–9 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: