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临床试验/EUCTR2008-000893-19-GB
EUCTR2008-000893-19-GB进行中(未招募)1 期

A randomised, double blind, placebo controlled, crossover trial of the adjuvant properties of imipramine for the overactive bladder. - RCT of adjuvant imipramine for the overactive bladder

Whittington NHS Trust0 个研究点目标入组 40 人开始时间: 2008年6月17日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
40

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

入选标准

  • 1. Adults aged 18 years or older
  • 2. Both males and females
  • 3. Symptoms of frequency more than or equal to 8 per day; urgency with or without urge incontinence
  • 4 On antimuscarinic montherapy for overactive bladder symptoms
  • 4. Able to give informed consent
  • 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) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1)<18 years
  • 2)Inability to provide consent.
  • 3)Current urinary infection as determined by >10 wbcs per ml onmicroscopy or 10^5 colony forming organisms on MSU.
  • 4) History of mania.
  • 5) Has taken monoamine oxidase inhibitors in the last 3 months.
  • 6) Myocardial infraction in the previous 6 months.
  • 7) Cadiovascular disease
  • 8) History of cardiac arrythmias.
  • 9) History of active liver disease
  • 10) Deranged liver function tests.
  • 11) Pregnant or breast feeding
  • 12) Heart Block
  • 13) Porphyria
  • 14) Open angle glaucoma
  • 15) Baldder cancer
  • 16) Prostate cancer
  • 17) Patients currently taking antidepressants with the exception of serotonin reuptake inhibitors or serotonin/noradrenaline reuptake inhibitors.
  • 18) Hyperthyroidism

研究者

发起方
Whittington NHS Trust

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