跳至主要内容
临床试验/JPRN-UMIN000028788
JPRN-UMIN000028788已完成未知

Clinical study of sensory evaluation using edoxaban orally disintegrating tablet (OD tablet) - Sensory evaluation study of edoxaban OD tablet

Daiichi Sankyo Co., Ltd. Medical Science Department0 个研究点目标入组 100 人开始时间: 2017年8月24日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
100

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)Patients who are taking dual anti-platelet therapy. 2)Patients who have experienced any cardiovascular events (stroke, myocardial infarction, cardiac intervention for cardiac events other than myocardial infarction, or heart failure requiring hospitalization) or any bleeding leading to hospitalization within two weeks before enrollment. 3) Patients who are pregnant or breast-feeding, or who have possibility to be pregnant. 4) Patients who are judged unsuitable for this study by the investigators.

研究者

发起方
Daiichi Sankyo Co., Ltd. Medical Science Department

相似试验