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临床试验/JPRN-UMIN000036773
JPRN-UMIN000036773已完成未知

Efficacy test of supplement containing plant extract - Efficacy test of supplement containing plant extract

KYOWA TRIAL CO., LTD0 个研究点目标入组 44 人开始时间: 2020年5月15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
44

研究概览

简要总结

A significant difference was observed in the primary outcome.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 64years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Those who have difficulty participating in the study due to liver, kidney, heart disease, respi ratory disorder, endocrine disorder, metabolic disorder, neurological disorder, consciousness disorder, diabetes (according to the criteria establ ished by the Japan Diabetes Association), and o ther diseases 2) Person with a history of cardiovascular disease 3) Those who are taking glucose metabolism, lipid metabolism, blood pressure improvement drugs 4) Those who regularly use medicines and health foods / supplements (including foods for specified health, functional labeling foods and nutritionally functional foods) that may affect this study (but stop taking it at the time of obtaining consent) The person who can do it does not correspond) 5) Persons who have allergies related to the test food 6) Those who have experienced poor mood or physical condition by blood collection in the past 7) Those who donated more than 200 mL from the month before the start of the test to the start of the test 8) Those who are participating in other clinical trials or within 4 weeks after the trial 9) Alcoholic drinkers and excessive smokers 10) Eating habits are extremely irregular 11) Those who wish to become pregnant during the study period, pregnant women (including those who may be pregnant) or those who are lact ating 12) Those who can not agree with the purpose of the description of this exam that is conducted in advance In addition, those who were judged inappropriate for this study by the study investigator

研究者

发起方
KYOWA TRIAL CO., LTD

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