KCT0003872已完成未知
A human study to evaluate the effect and the safety of GUCO on blood triglyceride levels
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 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
- Interventional Study
入排标准
- 年龄范围
- 20(Year) 至 0No Limit（—）
- 性别
- All
入选标准
- •1) Subject who voluntarily agree to participate and signs informed consent form
- •2) Men and women over 20 years old (ratio of men and women 1:1)
- •3) 150 mg/dL =Blood triglyceride levels <200 mg/d
排除标准
- •1) Excessive exercise (= 10 hours/week)
- •2) Heavy smoking (= 20 cigarettes/day)
- •3) Alcoholism or alcohol consumption more than 420g/week (soju 7 bottles/week)
- •4) BMI (Body Mass Index) <20.0 kg/m2 or =35.0 kg/m2
- •5) Recommended food score >36
- •6) Following diseases
- •: hyperlipidemia, diabetes, hypertension, liver disease, intestinal disease(inflammatory disease, lactose intolerance, etc), renal disease, cardiovascular disease, cerebrovascular disease, pancreatitis, cancer, thyroid disease, dementia, Parkinson's disease, depression, anorexia/bulimia, multiple sclerosis, spine injury, hypokalemia, uerine disease, etc.
- •7) Following medicines within 1 month before the first visit or during study,
- •: lipid-lowering agents(ursodeoxycholic acid), statin, etc), blood glucose-lowering drugs, antibiotics, drugs on intestine function, hormones, oral contraceptives, appetite depressants/stimulant, diuretics, beta-blockers, contraceptives, steroids, tricyclic antidepressants, laxatives, antidepressants, et al. But subjects taking thiazide or beta-blockers with no dose change for 1 year and during study can be enrolled.
- •8) Continuous consumption of oriental herbal medicine within 1 month before the first visit
- •9) Continuous consumption of dietary supplements with efficacy on blood lipids, blood glucose, body fat metabolism within 1 month before the first visit (phytosterol, omega-3 fatty acids, psyllium husk, aloe, chitosan, onion extract, nondigestible maltodextrin, dietary fiber, etc)
- •10) Subjects with hypersensitivity to test materials
- •11) Participation in other human study within one month before the first visit
- •12) Pregnant or lactating women
- •13) Any condition that the principal investigator believes may put the subjects at undue risk
研究者
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