跳至主要内容
临床试验/JPRN-UMIN000050001
JPRN-UMIN000050001尚未招募Unknown

Validation study of the effects on gut microenvironment by test-beverage intakes - Validation study of the effects on gut microenvironment by test-beverage intakes

CPCC Company Limited0 个研究点目标入组 120 人开始时间: 2024年1月14日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
120

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

  • Subjects - - (1) who take in affecting health-specific/functional/supplementary/health foods, lactic acid drinks (including yogurt drinks), or bifidobacterial beverages, over twice a week, (2) who take in yogurt, over 3 times a week, (3) who take in oligosaccharide and dietary fiber, over twice a week, (4) not having a habit of drinking milk, over once a week, (5) who have taken affecting medicines (gut/digestive/constipation/laxative regulation), over once a week, (6) having loose stools, owing to milk or cold beverage ingestion, (7) having a tendency to repeat constipation and diarrhea, (8) having a tendency to increase a defecation frequency by continuous intakes of water (0.1 L), (9) having constipation and diarrhea, owing to a menstruation, (10) with over 30.0 kg/m2 of BMI, (11) with frequency in going out, below twice a week, (12) with heavy smoking and excessive alcohol, (13) who have been on antibiotics after the pre-test to the hospital visiting (0 W), (14) planning to go on a long or trip abroad after the pre-test and during this study, (15) with extremely irregular eating habits / life rhythm, (16) having medical history of severe cardiac, hepatic, renal or digestive diseases, (17) with pregnancy, possibly one, or lactating, (18) having drug and food allergy (especially to milk and soybean), (19) being under another clinical test with medicine or health food, or partook in that within the past 4 weeks, or will partake in that after the consent, (20) who donated their blood components or blood (0.2 L) within the last month, (21) who donated his blood (0.4 L) within the past 3 months, (22) who donated her blood (0.4 L) within the past 4 months, (23) being collected in total of his blood (1.2 L) within the past 12 months and in this study, (24) being collected in total of her blood (0.8 L) within the past 12 months and in this study, (25) determined as ineligible for participation, judging from the principal/sub investigator - - .

研究者

发起方
CPCC Company Limited

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