KCT0002551招募中未知
A 8 week, randomized, double-blind, placebo-controlled clinical trial of APGP for the evaluation of efficacy on immune function and immune cell activation
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 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
- 25(Year) 至 75(Year)（—）
- 性别
- All
入选标准
- •1) Male or female subjects aged from 25 to 75 years old
- •2) Screening white blood cell(WBC) ranged from 4X103to 8X103cells/ul
- •3) Stress self assessment scaled above "strong"(4 scales: none, moderate, strong, intense)
- •4) Subjects who agreed to participate in this study and signed written informed consent voluntarily
排除标准
- •1) Subjects who are currently in the treatment of significant clinical disease related to acute or chronic cardiovascular system, immune system, respiratory system, liver biliary, kidney and urinary tract, nervous system, musculoskeletal disorders, psychic, infection and blood neoplastic. (However, subjects are possible to participate in the study by the discretion of the study director)
- •2) Subjects who have uncontrolled high blood pressure. (Higher than 140/90mmHg, measured 10 minutes after stabilizing)
- •3) Patients with uncontrolled diabetes. (126mg/dl or higher fasting glucose, or beginning of a new drug within 3months due to diabetes)
- •4) Subjects who got a vaccination within 3months before the screening.
- •5) Subjects whose ALT (GOT) or AST (GPT) exceeds two times the upper limit of normal levels (ULN)
- •6) Subjects whose blood creatinine level exceeds 1.5 times upper limit of normal levels (ULN)
- •7) Subjects who have taken or is taking functional foods that have the potential of affecting the immune system.
- •8) Subjects who have complained of severe gastrointestinal symptoms such as heartburn, indigestion.
- •9) Subjects who are planning a pregnancy, breastfeeding during this study.
- •10) Subjects who are sensitive to foods or have food allergies.
- •11) Subjects who are planning to participate other studies during this study.
- •12) Subjects who were involved in other human applied studies within 4weeks of this study begins.
- •13) Subjects who are deemed to be inappropriate to this human applied study.
研究者
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