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临床试验/JPRN-UMIN000008076
JPRN-UMIN000008076已完成4 期

Clinical Performance of the Endeavor Zotarolimus-Eluting Stent in Real-world Japanese Patients: A Prospective Multicenter Registry - E-KANSAI Registry

Associations for Establishment of Evidence in Interventions0 个研究点目标入组 1,000 人开始时间: 2012年6月4日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
1,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Women known to be pregant or lactating mothers. 2. Known hypersensitivity or allergy to drugs including aspirin, heparin, clopidogrel, ticlopidine, and ABT- 578; rapamycin, tacrolimus, sirolimus, or their analogues, or other analogues/derivatives; or cobalt, chrome, nickel, molybdenum, or contrast media. 3. Life expectancy estimated to be less than 12 months. 4. Acute myocardial infarction (AMI) accompanied by cardiogenic shock. 5. Preexisting stents (drug-eluting stents [DES] or bare metal stents [BMS]) in the target vessel (stents in a branch of the target vessel do not preclude enrollment). 6. Patients known to have difficulty in continuing dual antiplatelet therapy (DAPT) because of a plan of other surgery after stenting.

研究者

发起方
Associations for Establishment of Evidence in Interventions

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