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临床试验/JPRN-UMIN000026779
JPRN-UMIN000026779已完成未知

Effect of soy peptide supplementation on cognitive function -A paralleled, randomized, double-blind, placebo-controlled dose response study- - Effect of soy peptide on cognitive function

Miura Clinic, Medical Corporation Kanonkai0 个研究点目标入组 60 人开始时间: 2017年3月30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
60

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
60years-old 至 70years-old(—)
性别
Male

入选标准

  • 未提供

排除标准

  • 1)Patient with Alzhheimer's desease 2)Patient with food, drug, and/or specifically soy allergy 3)Patient who had treatment, hospitalization, and/or surgery due to Stroke, Subarachnoid hemorrhage, Cerebral infarction, Cerebral hemorrhage, Brain contusion, and/or Head trauma 4)Patient who ingested in excessive alcohol 5)Patient with chronic or acute infection 6)Patient who has current disease or history of hepatitis 7)Patient with dementia 8)Patient who are attending a hospital by following diseases or has medical history of Attack, Seizures, Diabetes, Thyroid dysfunction, Blood dialysis, Uremia, Anuria, Inner ear disease (Meniere's disease and so on), and/or Asthma 9)Patient with medical history of serious disorder (Liver disease, Kidney disease, Hypertension, Ischemic heart disease, Impaired glucose tolerance and so on) 10)Patient who has received the neuropsychological tests in hospital 11)Patient with movement disorders, visual impairment, hearing impairment 12)Patient who has experience to feel sick by watching shiny light 13)Patient on a diet 14)Patient with excessive smoking habit 15)Patient who has habitual intake of pharmaceuticals and foods (general food, dietary supplement, functional food, health food, food for health claims, beverage, confectionary and so on) which may affect test results 16)Patient participating in other clinical trials at the start of the present study 17)Patient who the investigator deems inappropriate

研究者

发起方
Miura Clinic, Medical Corporation Kanonkai

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