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临床试验/JPRN-UMIN000041019
JPRN-UMIN000041019已完成未知

A randomized and placebo-controlled double-blind, parallel-group study to investigate the cognitive efficacy of ascidian plasmalogens, - A randomized and placebo-controlled double-blind, parallel-group study to investigate the cognitive efficacy of ascidian plasmalogens,

Clinical Creative Corporation0 个研究点目标入组 146 人开始时间: 2020年8月18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
146

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
40years-old 至 75years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Persons taking medication for treatment of diseases (arrhythmia, liver damage, kidney damage, cerebrovascular disease, rheumatism, diabetes, dyslipidemia, hypertension and other chronic diseases) 2.Patients with malignancy, heart failure, or myocardial infarction, or who are undergoing treatment or have a history of such treatment 3.A person suffering from dementia 4.Those suffering from mental illnesses such as depression or attention deficit/hyperactivity disorder (ADHD) 5.Persons with allergies (pharmaceuticals and test foods) 6.Those who regularly consume foods or supplements that contribute to improving cognitive function, such as DHA, EPA, Ginkgo biloba extract, tocotrienol, astaxanthin, GABA, phosphatidylserine, lutein, zeaxanthin, imidazole dipeptides (carnosine, enserine, valenine), histidine, curcumin, bacopa saponin, lactonadecapeptide, anthocyanin, seryl tyrosine, auraptene, and diosgenin. 7.Persons who regularly consume pharmaceuticals (including herbal medicines), food for specified health uses, functional foods, or other foods/beverages with possible functional properties. 8.A person who has participated in another clinical trial within one month prior to obtaining consent or who is currently participating in another clinical trial. Those who, in the judgment of the principal investigator or sub-investigator, the conduct of the study may increase the risk to research subjects or may not provide sufficient data

研究者

发起方
Clinical Creative Corporation

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