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临床试验/JPRN-UMIN000033577
JPRN-UMIN000033577招募中未知

Efficacy and safety of tolvaptan in patients with severe aortic stenosis and chronic kidney disease undergoing transcatheter aortic valve replacement - TOlvaptan in Patients with severe aortic Stenosis undergoing Transcatheter Aortic valve Replacement (TOPSTAR)

Tokyo Women's Medical University0 个研究点目标入组 40 人开始时间: 2018年7月31日最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
40

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

  • Patients who violate the following criteria are excluded from this study 1 Patients receiving hemodialysis therapy 2 patients already taking tolvaptan 3 Patients with difficult oral medication 4 Patients who do not feel dry mouth 5 Those whose serum sodium level measured within 24 hours before the start of the study drug exceeds 150 mEq / ml 6 In addition, patients whose research managers judged inappropriate as subjects

研究者

发起方
Tokyo Women's Medical University

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