跳至主要内容
临床试验/JPRN-UMIN000016387
JPRN-UMIN000016387招募中4 期

Special Drug Use Surveillance of LIXIANA Tablet- Long-term use in patients with venous thromboembolism

DAIICHI SANKYO COMPANY, LIMITED0 个研究点目标入组 1,500 人开始时间: 2015年1月30日最近更新:

试验速览

阶段
4 期
状态
招募中
入组人数
1,500

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 meet the following requirements when starting to receive LIXIANA (at the time of enrollment for [3]) will be considered for admission to the study:
  • [1] Patients who have just started to receive LIXIANA for the first time for the treatment and secondary (recurrence) prevention of VTE (DVT and PTE)
  • [2] Patients who are to start treatment with LIXIANA during the period of contract (as per the signed contract between the institution and the sponsor) and during the enrollment period
  • [3] Patients who have given written informed consent to the study

排除标准

  • 未提供

研究者

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