跳至主要内容
临床试验/JPRN-UMIN000019164
JPRN-UMIN000019164已完成未知

Efficacy and Safety of Low Dose Prasugrel in Japanese Acute Coronary Syndrome Patients: A Single-center Prospective Clinical Trial - Efficacy and Safety of Low Dose Prasugrel

Kurashiki Central Hospital0 个研究点目标入组 250 人开始时间: 2015年9月30日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
250

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

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1) bleeding patients (hemophilia, cerebral bleeding, gastrointestinal bleeding, urinary tract bleeding, hemoptysis, or vitreous hemorrhage) (2) hypersensitive patients for prasugrel in past times (Relative exclusion criteria) (1) patients with cerebral bleeding or critical bleeding (BARC classification 3 or greater) (2) patients with past history of cerebral infarction or transient ischemic attack (3) patients with anticoagulant therapy or scheduled for anticoagulant therapy (4) patients with thienopyridine therapy already

研究者

相似试验