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临床试验/JPRN-UMIN000008257
JPRN-UMIN000008257尚未招募未知

A study to evaluate the efficacy and safety of Tolvaptan and Carperitide in HF patients - A study to evaluate the efficacy and safety of Tolvaptan and Carperitide in HF patients

Yokohama Sakae Kyosai Hospital0 个研究点目标入组 20 人开始时间: 2012年7月1日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
20

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) history of allergy against this drug or similar compounds (2) anuric patients (3) patients who cannot feel thirsty or have difficulty to drink (4) hypernatremia patients (5) patients who are pregnant or possibly pregnant (6) patients who already have tolvaptan at entry (7) acute myocardial infarction patients or planned revascularization during study period (8) patiets who administer intravenous diuretics except carperitide (9) patients who are judged to be inappropriate to this study

研究者

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