KCT0008862招募中Unknown
A 4 weeks, randomized, double-blind human trial to evaluate the efficacy and safety of Fermented soybean(Doenjang powder) on intestinal microflora and improvement of blood cholesterol
适应症
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 入组人数
- 45
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
- 19(Year) 至 75(Year)（—）
- 性别
- All
入选标准
- •1) Adult men and women aged 19 years or older and 75 years old or younger at the screening test.
- •2) Subjects with an LDL-cholesterol of 130 mg/dL or more or a total cholesterol of 200 mg/dL or more in a fasting blood test at the screening test.
排除标准
- •1) Those with clinically significant acute or chronic cardiocerebrovascular, endocrine, immune, respiratory, hepatobiliary, renal and urinary, neuropsychiatric, musculoskeletal, inflammatory and hematologic neoplastic, gastrointestinal, systemic and infectious diseases requiring treatment.
- •2) Those who have taken medicines and health functional foods related to improving intestinal flora and cholesterol within 1 month before screening
- •3) Those who are taking diabetes medications at the screening test.
- •4) Patients with uncontrolled hypertension at the screening test.
- •5) Those who have received antipsychotic drug treatment within 3 months prior to screening test.
- •6) Those with or suspected of alcoholism or drug abuse
- •7) pregnant or lactating women
- •8) Women of childbearing potential who do not accept the practice of adequate contraception
- •9) Those who participated in other human application tests within 3 months prior to screening test.
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