跳至主要内容
临床试验/JPRN-UMIN000024013
JPRN-UMIN000024013已完成未知

A clinical study for evaluating the efficacy of "Zendamakin-no-chikara" containing Lactcoccus lactis subsp. Cremoris FC on fanction of intestinal bacterial flora regulation. -Randomised double-blind placebo-controlled trial - A clinical study for evaluating the efficacy of "Zendamakin-no-chikara" containing Lactcoccus lactis subsp. Cremoris FC on fanction of intestinal bacterial flora regulation. -Randomised double-blind placebo-controlled trial

KSO Corporation0 个研究点目标入组 50 人开始时间: 2016年9月16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
50

研究概览

简要总结

The continuous ingestion of L. lactis subsp. cremoris FC caused changes in intestinal microflora, improving defecation status and fecal characteristics in healthy subjects prone to constipation.

研究设计

研究类型
Interventional

入排标准

年龄范围
30years-old 至 60years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1)Individuals taking antiflatulents and/or laxatives(including purgative drugs) in common use (2)Individuals taking health foods in common use, including food for specified health use, which influence intestinal regulation at the point of screening examination (3)Individuals taking antibiotics and/or drugs which influence laxatives(including purgative drugs) in common use at the point of screening examination (4)Individuals daily consuming alcohol as equivalent amount of sake more than 360ml (5)Individuals who are not able to stop consumption of foods containing lactic acid bacteria, bifidobacteria, natto bacteria, oligosaccharides, dietary fibers, high amount of sugar alcohol and/or other health foods including food for specified health use, which influence intestinal regulation during the study period (6)Individuals presenting known food allergy (7)Individuals who are suffered from a disease which needs treatment urgently or individuals with severe complications (8)Individuals with a digestive organ disease or surgical history who has an influence on digestive absorption and defecation (9)Individuals infected with a disease to urgently need treatment, or having serious complications (10)Individuals who are pregnant or breast-feeding, or have the will of pregnancy during the study period (11)Individuals who participate in other clinical studies or who are in willing to participate to these studies using foods, drugs and/or cosmetics (12)Individuals who are judged as unsuitable for the study by the investigator for the other reasons

研究者

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