Clinical Research Detail
Title Of Study This multicenter, prospective, observational registry will evaluate the safety and performance of the CYPHER SELECT Sirolimus-eluting Coronary Stent, and of all future generation of commercially approved Cordis Sirolimus-eluting Stents (SES), in routine clinical practice.
Disease Condition This registry will be limited to subjects who have received only the CYPHER SELECT Sirolimus-eluting Coronary Stent during the index procedure
Phase of Trial Phase-4 Discipline Cardiology
Start date of Trial 5/1/2006 Closing Date of Trial 5/1/2009
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