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临床试验/JPRN-UMIN000036381
JPRN-UMIN000036381已完成未知

Effect of supplement involved ferulic acid, glycerophosphocholine, ginkgo leaf extract and vitamin C on mild cognitive impairment. -Before after study- - A clinical trial to study the effect of supplement on mild cognitive impairment.

FANCL Corporation0 个研究点目标入组 40 人开始时间: 2019年4月4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
40

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
55years-old 至 74years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Subjects who constantly use Kampo preparation affecting cognitive function or dementia. 2) Subjects who constantly use supplements preparation affecting cognitive function or dementia. 3) Subjects who have psychiatric disorder affecting cognitive function or dementia with the exception of complete remission. 4)Subjects who take medical treatment for psychoneurosiswith antipsychotic drug. 5) Subjects with metabolic disease affecting cognitive function or dementia. 6) Subjects with liver disease, renal disease or hypoactivity of renal function (eGFR<=20 mL/min). 7) Subjects with uncontrolled type 2 diabetes or received insulin treatment. 8) Subjects with chronic obstructive lung disease and oxygen therapy in home or FEV1<30%. 9) Subjects with essential hypertension or uncontrolled hyperlipidemia. 10) Subjects who have medical history of gastrointestinal surgery or hospitalization for head injury within 10 years. 11) Subjects who have history of intracerebral hemorrhage, subarachnoid hemorrhage, cardiac hypertrophy, cardiac failure, ischemic heart disease, nephrosclerosis, aortic dissection or cerebral infarction. 12) Subjects with structural diseases with a possibility related to recognition dysfunction in the head MRI image acquired within 1 year before agreement acquisition or the first time check point. 13) Subjects who take medical treatment for cancer. 14) Subjects who are planned to participate in other clinical study. 15) Subjects who are judged as unsuitable for the study by the investigator for other reason.

研究者

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