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临床试验/EUCTR2009-013485-23-DE
EUCTR2009-013485-23-DE进行中(未招募)不适用

A Multicentre, Double-blind, Placebo-Controlled, Parallel Group Study of the Effect of Oral Etamsylate (Dicynone®) in Patients with Menorrhagia

OM PHARMA0 个研究点目标入组 230 人开始时间: 2009年12月2日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
230

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • Females aged = 18 to = 50, with excessive menstrual blood loss of = 80 to = 250 mL per menstruation and regular menstrual cycle.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients with systemic pathology which can influence haemostasis, patients with complex hyperplasia with or w/o atypia, endometrial carcinoma, severe adenomyosis or with submucous fibroids, patients with uterine cavity > 10 weeks of pregnancy size, patients pregnant or lactating and unreliable patients.

研究者

发起方
OM PHARMA

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