Status:
COMPLETED
CYPHERTM Stent Post-Marketing Surveillance Registry (US-PMS)
Lead Sponsor:
Cordis US Corp.
Conditions:
Coronary Artery Disease
Eligibility:
All Genders
Phase:
PHASE4
Brief 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...
Eligibility Criteria
Inclusion
- Cypher stent
Exclusion
- N/A
Key Trial Info
Start Date :
August 1 2003
Trial Type :
INTERVENTIONAL
End Date :
December 1 2004
Estimated Enrollment :
2070 Patients enrolled
Trial Details
Trial ID
NCT00245401
Start Date
August 1 2003
End Date
December 1 2004
Last Update
April 4 2007
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