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临床试验/JPRN-jRCT1080222253
JPRN-jRCT1080222253未知Unknown

iovel Combination Tablets special drug use surveillance Long-term use in patients with type 2 diabetes mellitus

TAKEDA PHARMACEUTICAL COMPANY LTD.0 个研究点目标入组 3,000 人开始时间: 2013年10月10日最近更新:

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

  • Patients with type 2 diabetes mellitus

排除标准

  • Patients meeting any of the following criteria will be excluded:
  • 1. Patients with current cardiac failure or a past history of cardiac failure
  • 2. Patients with severe ketosis, diabetic coma or precoma, or type 1 diabetes mellitus
  • 3. Patients with serious hepatic dysfunction
  • 4. Patients with serious renal dysfunction
  • 5. Patients with severe infection, pre- or post-operative patients, or patients with serious traumatic injury
  • 6. Patients with a history of hypersensitivity to any ingredients of Liovel
  • 7. Pregnant or possibly pregnant wome

研究者

发起方
TAKEDA PHARMACEUTICAL COMPANY LTD.

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