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临床试验/JPRN-UMIN000013220
JPRN-UMIN000013220已完成未知

Effect of the iron-lactoferrin complex on women with primary dysmenorrhea - Effectiveness of the iron-lactoferrin complex on dysmenorrhea

Soiken Inc.0 个研究点目标入组 25 人开始时间: 2014年2月22日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
Soiken Inc.
入组人数
25

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 50years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1) Subject having medical treatment in a hospital or clinic 2) Subject having treatment or previous history for serious cardiovascular, respiratory, endocrine, or metabolic disorders 3) Subject having any infectious diseases or their possibility 4) Subject who ended participation in another clinical trial less than 3 months before 5) Subject having cedar or cypress pollen allergy 6) Subject having a food allergy, specially dairy products 7) For female subjects: pregnancy or possibility of pregnancy, or intending to become pregnant during the study. 8) Subject who has had a blood sample of 200 ml or more taken (e.g., donated blood) within 1 month, or 400 ml or more within 3 months of the start of the present study 9) Subject deemed unsuitable by the investigator

研究者

发起方
Soiken Inc.

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