Trials / Completed
CompletedNCT00231244
Sirolimus-Eluting BX VELOCITYTM Balloon-Expandable Stent in a Compassionate Use Registry (SECURE)
Sirolimus-Eluting BX VELOCITYTM Balloon-Expandable Stent in a Compassionate Use Registry
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 252 (actual)
- Sponsor
- Cordis US Corp. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to allow treatment with the sirolimus-eluting Bx VELOCITYTM stent in patients with a serious disease or condition for which there is no generally acceptable alternate treatment available.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | CYPHER Sirolimus-Eluting Coronary Stent | CYPHER Sirolimus-Eluting Coronary Stent |
Timeline
- Start date
- 2002-03-01
- Primary completion
- 2008-05-01
- Completion
- 2008-11-01
- First posted
- 2005-10-04
- Last updated
- 2009-12-07
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00231244. Inclusion in this directory is not an endorsement.