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临床试验/EUCTR2008-002118-23-DE
EUCTR2008-002118-23-DE进行中(未招募)不适用

Studie zur Anwendung eines pflanzlichen Kombinationspräparats bei Frauen mit Reizblase (Overactive Bladder-Syndrom).(Translation: Study with a herbal combination in women with the overactive bladder syndrome (irritable bladder)). - femina-Studie (Translation:femina-study)

GlaxoSmithKline Consumer Healthcare GmbH & Co. KG0 个研究点开始时间: 2008年6月25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)

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

  • Women aged = 18 = 60 years
  • >= 8 micturions during 24 hours (average according diary over 3 days)
  • >= 1 episode of urge or urge incontinence in 24 hours (average according diary over 3 days)
  • overactive bladder symptoms consist since at least 3 months
  • 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

  • Diseases and conditions that may cause secondary irritable bladder or cause any other micturition complaints
  • Bladder cancer
  • Unexplained hematuria
  • Severe renal diseases
  • Severe hepatic diseases
  • Known hypersensitivity to ingredients of the study medication

研究者

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