JPRN-UMIN000044985已完成未知
Efficacy trial of 4 weeks ingestion of MSHF001 food - Efficacy trial of 4 weeks ingestion of MSHF001 food
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 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
- 40years-old 至 59years-old（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •-Subjects who are hot flashes 7 times a day or more, or 50 times a week or more. -Subjects with Kupperman index of 44 or higher. -Subjects with systemic illness. -Subjects who are diagnosed as menopausal disorders. -Subjects who are under Hormone Replacement Therapy (HRT). -Subjects who are outpatients or were treated by doctor within a month. -Subjects who are antidepressants, anxiolytics, hypnotic sedatives, taking drugs that affect psychiatric symptoms. -Subjects who have taken drugs or supplements (products mainly made with equol, isoflavones, and polyphenol-rich) that affect menopausal symptoms from 4 weeks before the screening trial. -Subjects who have been taking drugs or prescription drugs that affect the trial since 4 weeks before the start of the screening trial. -Subjects who are pregnant or lactating, or planned to become pregnant in the near future. -Subjects with smoking habit. -Subjects with drinking habit in every days (Alcohol equivalent 20g/day or more). -Subjects who have significantly disrupted the rhythm of their lives during the study period. -Subjects who have possibilities for emerging allergy to the ingredients contained in the test food, subjects with allergies such as drug allergy. -Subjects who plan to participate in other surveys or clinical trials between the time of recruitment and the end of the trial. -Subjects or their families engaged in the manufacture of health foods or supplements , market research company. -Subjects judged not appropriate by the physician responsible for the study.
研究者
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