跳至主要内容
临床试验/CTRI/2008/091/000170
CTRI/2008/091/000170已完成4 期

The e-SELECT Registry a MULTICENTER POST-MARKET SURVEILLANCEA multicenter prospective observational registry of the CYPHER SELECT Sirolimus- eluting Coronary Stent and of all future generation of commercially approved Cordis Sirolimus- eluting Stents.

Johnson and Johnson0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • This registry will be limited to subjects who have received only the CYPHER SELECT. Sirolimus-eluting Coronary Stent during the index procedure; Males and females; no inclusion or exclusion criteria have been specified, uniform, complete and accurate data will be collected peri-procedurally, during the index hospitalization, and during follow-up.

排除标准

  • 未提供

研究者

发起方
Johnson and Johnson

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