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临床试验/JPRN-UMIN000017908
JPRN-UMIN000017908已完成未知

The evaluation of the efficacy and the safety of TSUMURA Tokishakuyakusan Extract Granules for Ethical Use on endometriosis patients with dysmenorrhea - The effect of Tokishakuyakusan on endometriosis patients with dysmenorrhea

Tottori University Faculty of Medicine0 个研究点目标入组 15 人开始时间: 2015年6月15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 ot applicable(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1)Patients who have an abnormal genital hemorrhage which is not diagnosed or an endometrial polyp or an endometrial hyperplasia 2)Patients who have an extreme uterine swelling 3)Patients who need treatments other than LEP or patients who need surgery for endometriosis(including adenomyosis uteri) 4)Patients with serious complications (liver, kidney, heart, blood, or metabolic disorders) 5)Pregnant patients or patients who are probably pregnant 6)Breast-feeding patients 7)Patients who have allergy to Kampo medicine 8)Patients who have participated in other clinical trial or clinical research in the last three months at the point of acquiring consent 9)Patients who had treatments of hormonal drugs other than LEP (middle dose estrogen progesterone, GnRHagonist, LNG-IUS or Dienogest) in the last three months at the point of acquiring consent 10)Patients who had Kampo medicine treatment in the last four weeks at the point of acquiring consent 11)Patients who has changed the dosage and administration of limited concomitant drugs 12)Patients considered inappropriate by the study investigator

研究者

发起方
Tottori University Faculty of Medicine

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