跳至主要内容
临床试验/KCT0000568
KCT0000568终止未知

Morning to evening ratio in total dose of twice-daily biphasic insulin analog in achieving glucose control in patients with poorly controlled type 2 diabetes

Yonsei University Health System, Severance Hospital0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
终止
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
20(Year) 至 80(Year)(—)
性别
All

入选标准

  • 1) Subjects aged more than 20 years old
  • 2) Subjects with type 2 diabetes who were on sulphonylurea for glucose control
  • i) more than 7.5% A1c level at the time of enrollment
  • 3) Subjects who have willingness to keep the protocl
  • 4) Subjects who consent in written form

排除标准

  • 1) Cancer patients who currently on or will be scheduled for chemotherapy or radition therapy within 6 months.
  • 2) Subjects with renal failure who currently on or will be scheduled for hemodialyisis therapy within 6 months
  • 3) Subjects with heart failure (more than NYHA stage 3)
  • Subjects with liver failure (more than Child-Pugh class B)
  • 4) Gestational diabetes, type 1 diabetes and secondary yperglycemia, such as iatrogenic,inflammatory, or endocrine disorders, and liver cirrhosis.
  • 5) Subjects who do not consent the study

研究者

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