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临床试验/JPRN-UMIN000015112
JPRN-UMIN000015112已完成未知

A study of Luseogliflozin : the components of weight loss in the Japanese patients with type 2 diabetes mellitus

Regulatory mechanism of body composition through SGLT2 study group0 个研究点目标入组 48 人开始时间: 2014年9月10日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
48

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 65years-old(—)
性别
All

入选标准

  • 1) Patients with HbA1c (NGSP value) between 7.0% and 10.5% at the time of informed consent.
  • 2) Patients who have been receiving specific diet for more than 8 weeks at the time of initiation of luseogliflozin.
  • 3) Patients who have not taken any antidiabetes agents for more than 8 weeks or have been taking one oral hypoglycemic agent at the same dose.
  • 4) Patients with BMI between 20.0 and 35.0 at the time of informed consent.
  • 5) Patients (regardless of gender) who are aged 20 to 65 at the time of informed consent.
  • 6) Outpatients
  • 7) Patients who can receive an explanation before the participation in the study understand the contents and provide written informed consents by themselves.

排除标准

  • 1) Patients with diabetes mellitus other than type 2 diabetes mellitus (type 1 diabetes mellitus, diabetes mellitus due to specific mechanism/ diseases other than type 2 and gestational diabetes, etc.)
  • 2) Patients with severe renal impairment (nephrotic syndrome, renal failure and dialysis procedure, etc.)
  • 3) Patients with severe hepatic dysfunction (hepatic cirrhosis, etc.)
  • 4) Patients with severe cardiac disorder (cardiac failure, etc.), myocardial infarction and cerebral infarction or a previous history of these diseases within 6 months prior to the study
  • 5) Patients with severe diabetic microangiopathy (despite continuous treatment, inadequately-controlled diabetic retinopathy and diabetic neuropathy, etc.)
  • 6) Patients with malignant tumour or a previous history of malignant tumour (however, included those who were not treated for them, do not have recurrence and will not have a recurrence during the study can be included).
  • 7) Patients who have a previous history of hypersensitivity to luseogliflozin
  • 8) Severe chronic drinkers
  • 9) Pregnant or possibly pregnant women, women who hope to be pregnant and lactating women during the study
  • 10) Those considered inappropriate for the study by physicians in charge of the study

研究者

发起方
Regulatory mechanism of body composition through SGLT2 study group

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