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临床试验/JPRN-UMIN000038871
JPRN-UMIN000038871已完成未知

Efficacy trial of 4 weeks ingestion of the development code MSHF001 food - Efficacy trial of 4 weeks ingestion of the development code MSHF001 food

Kao Corporation0 个研究点目标入组 100 人开始时间: 2019年12月13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
100

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
20years-old 至 59years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • -Subjects with systemic illness. -Subjects who are diagnosed as menopausal disorders. -Subjects who are under Hormone Replacement Therapy, HRT, and/or medication which would affect blood hormone levels. -Subjects who are outpatients or were treated by doctor within a month. -Subjects who regularly take medicine. -Subjects who regularly take medicines that affect menopausal symptoms. -Subjects who are pregnant or lactating, or planned to become pregnant in the near future. -Subjects with smoking habit. -Subjects with drinking habit in 5 or more days a week. -Subjects who have possibilities for emerging allergy to foods, metals, and drugs. -Subjects with illnesses or diseases on their face, especially such as atopic dermatitis, or psoriasis, or severe acne. -Subjects who habitually having specific polyphenol-rich health food and drink. -Subjects with high anxiety questionnaire values. -Subjects with high Kupperman Kohnenki Shohgai Index. -Subjects who easily have skin rashes. -Subjects with potential conflict of interest.

研究者

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