Clinical trial
EPIC US Feasibility Study: Use of the FiberNet® Emboli Protection Device in…
NCT00346515 · Lumen Biomedical, Industry · Completed
Key facts
| NCT number | NCT00346515 |
|---|---|
| Title | EPIC US Feasibility Study: Use of the FiberNet® Emboli Protection Device in Carotid Artery Stenting |
| Official title | Evaluating the Use of the FiberNet® Emboli Protection Device in Carotid Artery Stenting: The EPIC US Feasibility Study |
| Lead sponsor | Lumen Biomedical, Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Carotid Artery Stenosis |
| Intervention type | Device |
| Interventions | FiberNet Emboli Protection System |
| Enrollment | 30 |
| Start date | Jun 1, 2006 |
| Completion | Jan 1, 2008 |
| First posted | Jun 30, 2006 |
| Last update posted | Oct 21, 2008 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No 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: