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临床试验/KCT0004641
KCT0004641尚未招募未知

Application of human body to confirm body fat improvement effect and safety of plant origin probiotics

Ewha Womans University0 个研究点目标入组 88 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
入组人数
88

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 63(Year)(—)
性别
All

入选标准

  • 1) Subject who voluntarily agree to participate and signs informed consent form
  • 2) Aged more than 19 years and less less than 65 years, women and men
  • 3) Those who have a body mass index (BMI) of 25kg/ bb m*2 or more and less than 30kg/m*2
  • 4) Those who can follow the diet and exercise guidelines during the intervention period

排除标准

  • 1) Those who have taken or are likely to take medications that affect body weight, blood sugar, lipids, or intestinal health within one month of the first visit
  • 2) Those who have taken antibiotics within 2 months of the first visit or are likely to take it during the study
  • 3) If you have,
  • 1.Uncontrolled hypertension
  • 2. Those who have been diagnosed with diabetes or are determined to need treatment, or who have fasting blood sugar
  • level of 180 mg / dL or more
  • 3. Liver dysfunction or hepatobiliary disease
  • 4. Renal dysfunction
  • 5. Hyperthyroidism and hypofunction, Cushing's syndrome
  • 6. If you have a medical history of severe central nervous system disorders that require hospitalization or medication
  • 7. Those with severe cerebrovascular disease, heart disease. However, dizziness
  • If there is no medical history, it may be excluded at the discretion of the researcher.
  • 8. Malignant tumor, lung disease, musculoskeletal disease, immune system or inflammatory disease
  • 9. A person who complains of gastrointestinal disorders or severe gastrointestinal symptoms such as heartburn,
  • indigestion or severe constipation
  • 10) Those who have continuously consumed dietary supplements or herbal medicines affecting their weight, blood sugar, and lipids within one month of their first visit.
  • 11) Those who have consistently consumed foods,Probiotics
  • 12) Those who have hypersensitivity to the test / control food or ingredients or have experienced severe food allergic
  • 13) Participants in other human application research within 1 month of first visit
  • 14) Pregnant or lactating women
  • 15) Those who have difficulty using a smartphone or computer
  • 16) If the researcher deems inappropriate to participate in this study

研究者

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