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临床试验/JPRN-UMIN000020201
JPRN-UMIN000020201已完成未知

Effect of daily ingestion of Kishu plum ( Prunus mume) on arteriosclerosis and lipid metabolism: a double-blind, placebo-controlled, parallel group comparison study. - Beneficial Effects of Daily Ingestion of Kishu plum on Arteriosclerosis and Lipid Metabolism

Hokkaido Information University0 个研究点目标入组 52 人开始时间: 2015年12月15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
52

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
35years-old 至 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Subjects who are under treatmentand medication for hyperlipidemia and diabetes. 2. Subjects with familial hypercholesterolemia. 3. Subjects whose LDL-C is >=180 mg/dl. 4. Subjects with serious cerebrovascular, cardiac, hepatic, renal, gastrointestinal diseases, disorder of endocrine and metabolism or affected with infectious diseases which are required to report to the authorities. 5. Subjects who have a major surgical history related to digestive system such as gastrectomy, gastrorrhaphy, enterectomy, etc. 6. Subjects with unusually high and/or low blood pressure or abnormal hematological data. 7. Subjects with serious anemia. 8. Pre- or post-menopausal women having obvious changes in physical condition. 9. Subjects who are at risk of having allergic reactions to drugs or foods (especially plum and agar). 10. Subjects who regularly take drugs, functional foods and/or supplements (EPA, DHA, MCT, phytosterol, sesamin, turmeric, polyphenols, dietary fiber, etc.) which would affect the blood lipid levels. 11. Subjects who regularly take drugs, functional foods and/or supplements (containing dietary fiber such as indigestible dextrin, polyphenol, etc.) which would affect blood glucose. 12. Heavy smokers, alcohol addicts or subjects with irregular lifestyle 13. Subjects who donate either 400ml whole blood within 12 weeks or 200ml whole blood within 4 weeks or blood components within 2 weeks prior to this study. 14. Pregnant or lactating women or women expect to be pregnant during the clinical trial. 15. Subjects who participate in other clinical trials within the last one month prior to this study. 16. Any other medical reasons judged by the principal investigator

研究者

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