JPRN-UMIN000041529已完成未知
Confirmation test about improvements of intestinal environment and immune function by test-food intake - Confirmation test about improvements of intestinal environment and immune function by test-food intake
CPCC Company Limited0 个研究点目标入组 20 人开始时间: 2021年8月26日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 20
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
- 20years-old 至 65years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •(1) Subjects with some kind of medical treatment continuously. (2) Subjects who have used some kind of medicine that might affect their intestine-regulating and immune functions. (3) Subjects who have used the following foods that might affect their intestine-regulating and immune functions; health-specific, functional, supplemental, health foods. (4) All through this trial, subjects who have any difficulty in refraining from having denying/restricting foods. (5) Pregnant or possibly pregnant women, or lactating ones. (6) Subjects with previous and/or current medical history of serious diseases in heart, liver, kidney and/or digestive organs. (7) Subjects with excessive alcohol intake. (8) Subjects with extremely irregular life rhythms, and subjects with midnight work or irregular shift work. (9) Subjects with previous medical history of drug and/or food allergy (especially in a soybean). (10) Subjects who are now under the other clinical tests with some kind of medicine/food, or participated those tests within four weeks after the current trial. (11) Subjects who donated over 200 mL of their whole blood and/or blood components within a month to the current trial. (12) Male subjects who donated over 400 mL of their whole blood within the last three months to the current trial. (13) Female subjects who donated over 400 mL of their whole blood within the last four months to the current trial. (14) Male subjects who will be collected over 1200 mL in total of their blood within the last twelve months, after adding the planned sampling blood amounts in this trial. (15) Female subjects who will be collected over 800 mL in total of their blood within the last twelve months, after adding the planned sampling blood amounts in this trial. (16) Others who have been determined as ineligible for participation, according to the principal/sub investigator's opinions.
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