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临床试验/JPRN-UMIN000037601
JPRN-UMIN000037601已完成未知

Effect of Daily Ingestion of the raw spirulina on Bowel Movements: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study - Beneficial Effect of Daily Ingestion of the raw spirulina on Bowel Movements

Hokkaido Information University0 个研究点目标入组 20 人开始时间: 2019年8月6日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
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
40years-old 至 60years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1. Subjects with a clinical history of gastrointestinal cancer or currently under treatment or anti-tumor medication. 2. Subjects with gastrointestinal disorders such as inflammatory bowel syndrome, irritable bowel syndrome, etc. 3. Subjects with photosensitivity. 4. Subjects who regularly take anticoagulant, antiplatelet medicine, and/or NSAIDs. 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 such as gastrectomy, gastrorrhaphy, enterectomy, etc. 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 especially based on seaweed and gelatin. 11. Subjects who regularly take the food containing spirulina, young barley, euglena and/or chlorella. 12. Subjects who regularly take drugs, functional foods and/or supplements which potentially affect bowel movements. 13. Heavy smokers, alcohol addicts or subjects with disordered lifestyle. 14. 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 current study. 15. Pregnant or lactating women or women who expect to be pregnant during this study. 16. Subjects who currently participate in other clinical trials, or participated within the last 4 weeks prior to the current study. 17. 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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