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临床试验/JPRN-jRCT1080222234
JPRN-jRCT1080222234已完成Unknown

esina tablets special drug use surveillance: Mild type 2 diabetes mellitus

Takeda Pharmaceutical Company Limited0 个研究点目标入组 19,192 人开始时间: 2013年9月24日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
入组人数
19,192

研究概览

简要总结

This surveillance was conducted to examine the safety and efficacy of long-term Nesina therapy in patients with mild type 2 diabetes mellitus. The surveillance results raised no major concerns about the safety or efficacy of long-term Nesina therapy.

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 HbA1c (JDS value) less and equal 7.0% at the time of enrolment (within 3 months before initiation of Nesina therapy), regardless of the use of antidiabetic medication.

排除标准

  • Patients contraindicated for Nesina
  • (1) Patients with severe ketosis, diabetic coma or precoma, or type 1 diabetes mellitus.
  • (2) Patients with severe infection, pre- or post-operative patients, or patients with serious traumatic injury.
  • (3) Patients with a history of hypersensitivity to any ingredient of Nesina.

研究者

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