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临床试验/JPRN-UMIN000036578
JPRN-UMIN000036578已完成未知

Study 3 Verifying the Improving Effect of Green Tea Ingredients on Cognitive Function - Study 3 Verifying the Improving Effect of Green Tea Ingredients on Cognitive Function

HUMA R&D CORP0 个研究点目标入组 51 人开始时间: 2019年4月26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
51

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
50years-old 至 69years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Subject who is currently receiving any medications or outpatient treatment. 2)Subject who is currently doing exercise or diet under the supervision of a doctor 3)Subject who is may develop allergy due to the test food 4)Subject who is drug dependent, present or dependent on alcohol 5) Subject who is history of psychiatry during hospitalization due to mental disorder (depression etc.) or sleep disorder (insomnia, sleep apnea syndrome etc.) 6)Night shift or shift workers 7) Excessively irregular lifestyle such as eating or sleeping 8) Subject who is extreme skipped eating 9)Subject who is current disease or history of diabetes, liver disease (hepatitis), kidney disease, serious disease such as heart disease, thyroid disease, adrenal disease, other metabolic diseases 10)Subject who is use health foods, supplements, and medicines that may affect cognitive function 11) Subject who is participated in other human clinical studies within the past 3 months or are expected to participate in other human clinical studies during the study period. 12)Subject who is carried out blood collection, component blood donation more than 400 mL within 200 mL or 3 months within one month going back from the date of consent acquisition 13) Subject who is pregnant, breast-feeding, or willing to become pregnant during the study period 14)Subject who is difficult to comply with the records of various surveys 15)Subject who is judged to be unsuitable as subject from clinical laboratory test value and measurement value at the time of SCR 16)Other than the above, the principal investigator judged that the subject was ineligible for the study.

研究者

发起方
HUMA R&D CORP

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