Clinical trial
SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary…
NCT00180310 · Abbott Medical Devices, Industry · Completed
Key facts
| NCT number | NCT00180310 |
|---|---|
| Title | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary Stent System |
| Official title | A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary Stent System in the Treatment of Patients With de Novo Native Coronary Artery Lesions |
| Acronym | SPIRIT II |
| Lead sponsor | Abbott Medical Devices, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Coronary Disease, Coronary Artery Disease, Coronary Restenosis |
| Intervention type | Device |
| Interventions | XIENCE V® Everolimus Eluting Coronary Stent, TAXUS™ EXPRESS2™ Paclitaxel Eluting Coronary Stent |
| Enrollment | 300 |
| Start date | Jul 1, 2005 |
| Primary completion | Jul 1, 2007 |
| Completion | Feb 1, 2011 |
| First posted | Sep 16, 2005 |
| Last update posted | Jul 20, 2011 |
| Countries | Austria, Belgium, Denmark, France, Germany, India, Italy, Netherlands, New Zealand, Poland, South Africa, Spain and 1 more |
At a glance
- 10–99 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: