Trials / Completed
CompletedNCT00245401
CYPHERTM Stent Post-Marketing Surveillance Registry (US-PMS)
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 2,070 (planned)
- Sponsor
- Cordis US Corp. · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The purpose of this PMS registry, named e-CYPHER Stent Registry, is to collect post marketing surveillance data on the CYPHERTM Sirolimus-eluting Coronary Stent following marketing approval, when used in normal clinical practice within the labeled indications.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | CYPHERTM Sirolimus-Eluting Coronary Stent |
Timeline
- Start date
- 2003-08-01
- Completion
- 2004-12-01
- First posted
- 2005-10-28
- Last updated
- 2007-04-04
Source: ClinicalTrials.gov record NCT00245401. Inclusion in this directory is not an endorsement.