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临床试验/JPRN-jRCT1080222219
JPRN-jRCT1080222219未知Unknown

esina tablets special drug use surveillance Type 2 diabetes mellitus: Combination therapy with sulfonylurea

TAKEDA PHARMACEUTICAL COMPANY LTD.0 个研究点目标入组 1,000 人开始时间: 2013年9月10日最近更新:
适应症

试验速览

阶段
Unknown
发起方
入组人数
1,000

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 who did not adequately respond to the following treatment
  • Treatment with sulfonylurea in addition to diet therapy and exercise therapy

排除标准

  • Patients contraindicated for Nesina
  • (1) Patients with severe ketosis, diabetic coma or precoma, or type 1 diabetes mellitus [these patients require prompt adjustment of hyperglycemia by fluid infusion and insulin, and hence use of Nesina is not appropriate.]
  • (2) Patients with severe infection, pre- or post-operative patients, or patients with serious traumatic injury [blood glucose control by insulin injection is desirable for these patients, and hence use of Nesina is not appropriate.]
  • (3) Patients with a history of hypersensitivity to any ingredient of Nesina

研究者

发起方
TAKEDA PHARMACEUTICAL COMPANY LTD.

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