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临床试验/JPRN-jRCT2031220131
JPRN-jRCT2031220131招募中未知

Special drug use Surveillance for EFIENT Tablets- Patient with ischemic cerebrovascular disease with a high risk of ischemic stroke

Matsuoka Yomei0 个研究点目标入组 1,200 人开始时间: 2022年6月12日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
1,200

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
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • Patients who fulfilled the following criteria:
  • (1) Patients with ischemic cerebrovascular disease associated with large-artery atherosclerosis or small-vessel occlusion (restricted to cases with a high risk of ischemic stroke*1), who were administered EFIENT for the first time
  • *1: Patients with either hypertension, dyslipidemia, diabetes mellitus, chronic kidney disease or a history of ischemic stroke before the last episode of attack
  • (2) Patients who started administration of EFIENT tablet during the contract period (contract period based on the contract with each medical site) and until 30/June/2023
  • (3) Patients from whom written informed consent was obtained

排除标准

  • 未提供

研究者

发起方
Matsuoka Yomei

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