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临床试验/KCT0001434
KCT0001434已完成未知

A human study to evaluate safety and effective dose of Morus alba twig extract on postprandial glucose level in healthy subjects

Ewha Womans University0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
20(Year) 至 39(Year)(—)
性别
All

入选标准

  • 1) Age: 20 years = Age < 40 years
  • 2) FBG (Fasting Blood Glucose): < 126mg/dL

排除标准

  • 1) Continuous consumption of drug that affect glucose metabolism, inflammation, antioxidative capacity and lipid metabolism or dietary supplement or oriental medicine or within 4 weeks before the first visit
  • 2) Consumption of anticoagulant within 4 weeks before the first visit
  • 3) BMI=18.5 or BMI=30
  • 4) Following diseases :
  • ? Diagnosis of diabetes or fasting blood glucose = 126mg/dL at screening
  • ? Liver dysfunction (AST, ALT level elevations more than 2.5 times the upper limit of normal)
  • ? Renal dysfunction (serum creatinine = 1.4mg/dL)
  • ? Cardiovascular diseases (hypertension (= 140/90 mmHg), stroke, etc.)
  • ? Thyroid diseases, mental diseases such as depression, schizophrenia, alcoholism, drug addiction, wasting diseases such as malignant tumor etc., and severe muscular skeletal disease, asthma and allergic diseases, any condition that the principal investigator believes may put the subjects at undue risk
  • 5) Chronic smoker (= 20 cigarettes / day)
  • 6) Excessive exercise (= 10 hours / week)
  • 7) Change of body weight more than 4 kg or weight control within 4 weeks before the first visit
  • 8) Subjects with hypersensitivity to test materials
  • 9) Participation in other human study within 4 weeks before the first visit
  • 10) Pregnant or lactating women
  • 11) Any condition that the principal investigator believes may put the subjects at undue risk

研究者

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