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临床试验/JPRN-UMIN000034056
JPRN-UMIN000034056已完成未知

Efficacy trial of ingestion of the development code MSHFS001. - Efficacy trial of ingestion of the development code MSHFS001.

Kao Corporation0 个研究点目标入组 82 人开始时间: 2018年9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
82

研究概览

简要总结

The results show that continuous intake of CGAs resulted in improvements in menopausal symptoms, especially hot flushes, in healthy women.

研究设计

研究类型
Interventional

入排标准

年龄范围
40years-old 至 59years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • -Subjects who have been suffered from disease. -Subjects who regularly take medicine. -Subjects who are undergoing medical treatment or were treated by doctor within a month. -Subjects who are under hormone replacement therapy (HRT), and / or subjects who are in medication that affect blood hormone levels. -Subjects who regularly take supplements related to menopausal symptoms. -Subjects who regularly take functional food and/or supplements related to sleep. -Subjects who are pregnant, lactating, or planned to become pregnant during the test period. -Subjects with smoking habit. -Subjects who cannot follow the restriction of eating habit. -Subjects who have possibilities for emerging allergy to foods, metals, and drugs. -Subjects who are shift workers. -Subjects deemed inappropriate to participate in this study by the principle investigator.

研究者

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