跳至主要内容
临床试验/JPRN-jRCT2031230289
JPRN-jRCT2031230289招募中Unknown

Surveillance of ischemic stroke recurrence after prescription of EFIENT tablets (prasugrel)-JMDC Cohort Study

Matsuoka Yomei0 个研究点目标入组 1,300 人开始时间: 2023年8月12日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
1,300

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

  • 1) Patients who have prescription of prasugrel or clopidogrel within the enrollment period (December 24, 2021 to May 31, 2027). The cohort entry date: first prescription date of prasugrel or clopidogrel within the enrollment period.
  • 2) Patients with acute ischemic stroke treated in hospital have diagnosis of atherothrombotic stroke or lacunar stroke during the past 30 days from the day before the cohort entry date.
  • 3) Patients who have risk factors for ischemic stroke recurrence.
  • 4) Patients who have medical records for the past 90 days from the day before the cohort entry date (Look back period).

排除标准

  • 1) Patients who have prescription of prasugrel or clopidogrel in the look back period.
  • 2) No medical records from the day after the cohort entry date.
  • 3) Patients who have prescriptions of prasugrel and clopidogrel on the cohort entry date.

研究者

发起方
Matsuoka Yomei

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