Clinical trial
The Study of the BX VELOCITY Stent In Patients With De Novo Coronary Artery…
NCT00235144 · Cordis US Corp., Industry · Completed
Key facts
| NCT number | NCT00235144 |
|---|---|
| Title | The Study of the BX VELOCITY Stent In Patients With De Novo Coronary Artery Lesions. |
| Official title | E-Sirius Study: a European, Multi-Center, Randomized, Double-Blind Study of the Sirolimus-Coated BX VELOCITY Balloon-Expandable Stent in the Treatment of Patients With de Novo Coronary Artery Lesions |
| Acronym | E-SIRIUS |
| Lead sponsor | Cordis US Corp., Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Coronary Artery Disease |
| Intervention type | Device |
| Interventions | sirolimus-coated Bx Velocity stent, uncoated Bx Velocity stent |
| Enrollment | 353 |
| Start date | Mar 1, 2001 |
| Primary completion | Oct 1, 2002 |
| Completion | Sep 1, 2008 |
| First posted | Oct 10, 2005 |
| Last update posted | May 11, 2009 |
| Countries | Germany |
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: