JPRN-UMIN000039591已完成未知
A confirmation study of bowel control effect by consumption of the test food - A confirmation study of bowel control effect by consumption of the test food
CPCC Company Limited0 个研究点目标入组 40 人开始时间: 2021年2月28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
- 40
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 constantly eat seaweeds like simmered laver in sweetened soy sauce etc., or subjects who can't restrict eat them during test period. 2) Subjects who are given continuous treatment by taking medicines. 3) Subjects who intaking Food for Specified Health Uses (FOSHU), food with function claims and/or health food, those having possibility of defecation improvement or soft stool improvement, more than three days a week. 4) Females who are pregnant or lactating, and females who could become pregnant or lactating during test period. 5) Subjects who have previous and/or current medical history of serious disease (e.g., heart, liver, kidney, digestive organ). 6) Subjects who excessive alcohol intake. 7) Subjects who have extremely irregular dining habits, and subjects who have midnight work or irregular shift work. 8) Subjects who have previous medical history of drug and/or food allergy. 9) Subjects who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests. 10) Subjects who donated over 200mL blood and/or blood components within the last one month to the current study. 11) Males who donated over 400mL blood and/or blood components within the last three months to the current study. 12) Females who donated over 400mL blood and/or blood components within the last four months to the current study. 13) Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last twelve months are adding to the planned sampling amounts of this study. 14) Females who will be collected over 800mL blood and/or blood components when, the sampling amounts within the last twelve months are adding to the planned sampling amounts of this study. 15) Others who have been determined ineligible by principal investigator or sub-investigator.
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