跳至主要内容
临床试验/CTRI/2013/12/004227
CTRI/2013/12/004227Other4 期

GLucobay M - Evaluation Of Safety and Effectiveness in Type 2 Diabetes Not Well Controlled on Monotherapy in Real Life Practice - GLORY

Bayer Zydus Pharma0 个研究点目标入组 10,000 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
Other
发起方
入组人数
10,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Pms

入排标准

入选标准

  • Patient will be enrolled after the decision to administer acarbose/metformin fixed dose combination for type-2 diabetes management has been made by the attending physician on the basis of best clinical practice and patient needs.
  • Willing to give informed consent for participating in this study

排除标准

  • Patients receiving anti-diabetic medication other than acarbose, or metformin monotherapy at the time of enrollment in the study will be excluded. However, during observation period, any additional anti-diabetics medication administered by the attending physician will be allowed & recorded in case record form.
  • Patient receiving acarbose/metformin fixed dose combination during 3-months prior to enrollment.
  • Exclusion criteria should be read in conjunction with local product information

研究者

发起方
Bayer Zydus Pharma

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