JPRN-UMIN000044815已完成未知
Effect of Daily Intake of Test Food on Skin Function : A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study - Effect of Daily Intake of Test Food on Skin Function
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 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
- 30years-old 至 65years-old（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •1. Subjects who has symptoms of atopic dermatitis. 2. Subjects with a clinical history of gastrointestinal cancer or currently under treatment or anti-tumor medication. 3. Subjects with gastrointestinal disorders such as inflammatory bowel syndrome, irritable bowel syndrome, etc. 4. Subjects who has significant abnormal skin condition at the test site. 5. Subjects with serious cerebrovascular, cardiac, hepatic, renal, gastrointestinal diseases, and/or affected with infectious diseases requiring reports to the authorities. 6. Subjects with major surgical history relevant to the digestive system. 7. Subjects with unusually high and/or low blood pressure and/or abnormal hematological data. 8. Subjects with severe anemia. 9. Pre- or post-menopausal women complaining of obvious physical changes. 10. Subjects who are at risk of having allergic reactions to drugs or foods. 11. Subjects who could have a seasonal allergy during this study. 12. Subjects who use gastrointestinal drugs or female hormone once or more a week. 13. Subjects who regularly take functional foods and/or supplements which potentially affect bowel movements. 14. Subjects who regularly take fiber reinforced food and/or yogurt. 15. Subjects who have used or will use antimicrobials between 12 weeks prior to study entry and the end of the study. 16. Heavy smokers, alcohol addicts or subjects with disordered lifestyle. 17. Subjects who donated either 400 ml whole blood within 16 weeks, 200 ml whole blood within 4 weeks, or blood components within 2 weeks, prior to the study. 18. Pregnant or lactating women or women who expect to be pregnant during this study. 19. Subjects who currently participate in other clinical trials, or participated within the last 4 weeks prior to the study. 20. Any other medical and/or health reasons unfavorable to participation in the current study, as judged by the principal investigator.
研究者
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