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临床试验/JPRN-jRCT1080222313
JPRN-jRCT1080222313未知Unknown

ECARD Combination Tablets LD&HD special drug use surveillance: Long-term use (12 months)

TAKEDA PHARMACEUTICAL COMPANY LTD.0 个研究点目标入组 3,000 人开始时间: 2013年12月3日最近更新:
适应症

试验速览

阶段
Unknown
发起方
入组人数
3,000

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

  • Post-marketing surveillance

排除标准

  • (1) Patients with a history of hypersensitivity to ingredients of ECARD LD&HD combination tablets, thiazides, or their analogues (e.g. sulphonamide derivatives such as chlortalidone)
  • (2) Patients with anuria or patients under hemodialysis
  • (3) Patients with acute renal failure
  • (4) Patients with noticeably decreased Na and K levels in body fluids
  • (5) Pregnant women or women planning to become pregnant

研究者

发起方
TAKEDA PHARMACEUTICAL COMPANY LTD.

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