JPRN-UMIN000043979已完成未知
Verification of test food-ingesting effects on gut microbiota and IgA - Verification of test food-ingesting effects on gut microbiota and IgA
CPCC Company Limited0 个研究点目标入组 80 人开始时间: 2021年4月21日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 80
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 who have a plan or who have taken medication within a month before the trial start, which would affect the trial result. (2) Subjects who are regularly consuming food for specified health uses, food with function claims, supplement and/or health foods which would affects the trial results for more than 3 times a week. (3) Subjects who are regularly consuming mushrooms for not less than 6 days a week. (4) Subjects who have difficulty from restricting mushroom-intakes for less than 2 days a week, as well as less than 50 g a week. (5) Subjects who dislike mushrooms. (6) Subjects who had undergone appendectomy. (7) Subjects who have received the surgery which would affect the trial result within half a year before obtaining a consent. (8) Subjects who have previous/current medical history of severe cardiac, hepatic, renal or digestive diseases. (9) Pregnant, possibly pregnant, or lactating women. (10) Subjects who take excessive alcohol. (11) Subjects with irregular life style and irregular dietary habit. (12) Subjects who have food allergy. (13) Subjects who are planning to receive vaccination during this trial. (14) Subjects who are now under the other clinical tests with some kind of medicine/food, or took part in those within 4 weeks before this trial, or will join those after giving informed consent to participate in this trial. (15-17) Subjects who donated their blood components and/or whole blood as below - all subjects: 200 mL within a month - males: 400 mL within the last 3 months - females: 400 mL within the last 4 months to this trial. (18) Males who will be collected in total of their blood (1200 mL) within the last 12 months, after adding the blood amounts planning to be sampled in this trial. (19) Females who will be collected in total of their blood (800 mL) within the last 12 months, after adding the blood amounts planning to be sampled in this trial. (20) Others who have been determined ineligible by principal/sub investigator.
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