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临床试验/JPRN-UMIN000041648
JPRN-UMIN000041648已完成未知

Effect of Chlorella pyrenoidosa on Defecation -A Randomized, Double-blind, Cross-over-Study- - Effect of Chlorella pyrenoidosa on Defecation -A Randomized, Double-blind, Cross-over-Study

Sun Chlorella Corporation0 个研究点目标入组 40 人开始时间: 2020年9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
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 60years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • (1) Subjects who are continuously receiving treatment with medicines (2) Subjects who regularly takes food for specified health use, functional foods, health foods, etc. that may affect the test. (3) Subjects who are pregnant (including subjects who may be pregnant) or lactating. (4) Subjects who donate blood or collect 200 ml or more of whole blood from 4 weeks prior to the start of the clinical test. (5) Subjects who collect 400 ml or more of whole blood from 16 weeks prior to the start of the clinical test. (6) Subjects whose blood collection volume from the month 12 months prior to the start of the clinical test to the start of it, plus the total planned blood collection volume for the clinical test, exceeds 800 ml (7) Subjects currently participate as test subjects in another clinical test or have participated in the test within 4 weeks (8) Subjects with pain or bleeding during defecation (9) Subjects who underwent laparotomy within 6 months of the test (10) Subjects who took antibiotics within 6 months of the test (11) Subjects who drink too much alcohol and smoke excessively. (12) Subjects with extremely irregular eating habits, shift work or midnight shift (13) Subjects who plan to change their lifestyle substantially during the test period (14) Subjects who are chronically prone to diarrhea (15) Subjects who falls under any of the following (a) Subjects with heart, liver or kidney disease (including when it is a complication of another disease) (b) Subjects with a history of cardiovascular disease

研究者

发起方
Sun Chlorella Corporation

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