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临床试验/NL-OMON39367
NL-OMON39367已完成不适用

the Dutch Stent Thrombosis Study - DUST

Sint Antonius Ziekenhuis0 个研究点目标入组 4,000 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
4,000

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
18 至 99(—)

入选标准

  • all patients suffering a stent thrombosis

排除标准

  • Abcense of an informed consent.;If a case or matched control patient dies before written Informed Consent could be obtained the clinical data will be used for the study, but only if the researcher doesn*t have any suggestion that the patient would have declined his consent if he still would have been alive. The researcher will write a note in the CRF stating this assumption. The family will not be contacted and no blood samples will be stored.

研究者

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