JPRN-UMIN000044381已完成未知
Verification of the effects induced by test-food intakes on gut microenvironment and IgA - Verification of the effects induced by test-food intakes on gut microenvironment and IgA
CPCC Company Limited0 个研究点目标入组 68 人开始时间: 2021年6月2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
- 68
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 60years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •(1)Subjects who take cereal more than 3 times a week. (2)Subjects who have a plan or who have taken medication within a month before the trial start, which would affect the trial result. (3)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. (4)Subjects who cannot drink milk. (5)Subjects with lactose intolerance. (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)Subjects who are suspected of seriously chronic/acute infectious diseases. (10)Subjects who are planning to receive vaccination during this trial. (11)Pregnant, possibly pregnant, or lactating women. (12)Subjects who take excessive alcohol. (13)Subjects with smoking habit, now and/or within a year before this trial. (14)Subjects with irregular dietary habits. (15)Subjects whose roomer is planning to join this trial. (16)Subjects who are planning to change their life style considerably during this trial. (17)Subjects who have food allergies. (18)Subjects who are now under the other clinical tests with some kind of medicine/food, or participated in those within a month before this trial, or will join those after giving informed consent to participate in this trial. (19-21)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. (22-23)Subjects whose collected blood volume within the last 12 months would reach to following criteria after adding the blood collection in this study; - males: 1,200 mL - females: 800 mL (24)Others who have been determined ineligible by principal/sub investigator.
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