CYPHERTM Stent Post-Marketing Surveillance Registry (US-PMS)
NCT00245401 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 2070
Last updated 2007-04-04
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
- DEVICE
-
CYPHERTM Sirolimus-Eluting Coronary Stent
Sponsors & Collaborators
-
Cordis Corporation
lead INDUSTRY
Principal Investigators
-
Emerson Perin, MD · Texas Heart Institute
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2003-08-31
- Completion
- 2004-12-31
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