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临床试验/JPRN-UMIN000022829
JPRN-UMIN000022829已完成未知

A study of efficacy of plant-derived product in female with voiding dysfunction. - A study of efficacy of plant-derived product in female with voiding dysfunction.

TTC Co.,Ltd0 个研究点目标入组 15 人开始时间: 2017年12月31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
15

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 80years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1) LUTS/OAB patients or subjects who need to treatment of disease. 2) Subjects who have the habit of taking test food. 3) Subjects who have the habit of taking healthcare products. 4) Subjects who have a habit of binge drinking. 5) Patients who have serious disease or subjects who have serious disease history. 6) Subjects who take warfarin potassium or antacid. 7) Subjects who has allergies to plants. 8) Urinary calculus or bladder calculus. 9) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination. 10) Females who are known or suspected to be pregnant, breastfeeding or desire to become pregnant during the trial period. 11) Subjects who are participated in other clinical studies. 12) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire. 13) Subjects who are judged unfit to enroll in this trial by the investigator.

研究者

发起方
TTC Co.,Ltd

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