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临床试验/JPRN-UMIN000048861
JPRN-UMIN000048861尚未招募Unknown

Effects of supplements containing multiple ingredients on fasting blood glucose levels, triglyceride levels, and blood pressure in healthy subjects -A randomized, placebo-controlled, double-blind, parallel-group study - Effects of supplements containing multiple ingredients on fasting blood glucose levels, triglyceride levels, and blood pressure in healthy subjects -A randomized, placebo-controlled, double-blind, parallel-group study

Medical Corporation Hokubukai Utsukushigaoka Hospital0 个研究点目标入组 90 人开始时间: 2023年9月15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
90

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 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Subjects who have been diagnosed as metabolic syndrome 2)Subjects with a history of hepatic, renal, cardiac or organ disorders, diabetes or other serious diseases. 3) Subjects with a surgical history of digestive system (except appendicectomy). 4) Subjects currently under treatment with chronic diseases. 5) Subjects with food allergies to the food used in the study. 6) Subjects who wish to become pregnant during the study period or who are lactating or pregnant or may be pregnant. 7) Heavy drinkers (average amount of intake as pure alcohol is 60 g or more per day). 8)Subjects who take supplement emphasizing the inclusion of inulin, epigallocatechin, chlorogenic acid, epigallocatechin gallate, indigestible dextrin, 5-aminolevulinic acid, gallic acid, lactoferrin, mulberry leaf extract, salacia extract, kudzu flower extract, African mango tree extract, DHA / EPA, or rose hip extract or general health foods(e.g., protein diet) for 3 days or more per week and have continued to take it for 6 months or more T, and who cannot stop taking it during the study period . 9) Subjects taking the medicines (e.g., the Bislat Gold EX or the Naishitol Zaf), the Chinese medicine (e.g., the Bofutsushosan or the Daisaikoto) or the supplements claiming for the reduction of the body fat on diet. 10) Subjects who are participating in clinical trials or consumer monitoring other than this study or who are planning to participate during this study period. 11) Subjects who have donated 200 ml or more of blood after 1 month before the primary screening or plan to donate them before the end of the study. 12) Subjects who frequently skip breakfast. 13) Subjects who work during 22:00 to 6:00 (shift worker, night- shift worker, etc.). 14) Subject who need to avoid consuming food whose origin is not clearly indicated due to religious or other reasons. 15) Subjects judged as unsuitable for this study by the investigator with other reasons.

研究者

发起方
Medical Corporation Hokubukai Utsukushigaoka Hospital

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