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临床试验/ACTRN12611000828921
ACTRN12611000828921终止3 期

A randomised controlled trial comparing the proportion of patients with daytime incontinence cured at 3 months by the personal alarm watch versus a conventional watch to aid timed voiding

The Children's Hospital at Westmad0 个研究点目标入组 360 人开始时间: 2011年8月5日最近更新:
适应症

试验速览

阶段
3 期
状态
终止
发起方
入组人数
360

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
5 Years 至 13 Years(—)
性别
All

入选标准

  • Children aged 5 to 13 years who have DUI at least twice per week (in the past 2 weeks) for which a timed voiding program is indicated

排除标准

  • Children with an organic cause for DUI including defects of central nervous system or underlying urological abnormality or where a timed voiding program is contraindicated

研究者

发起方
The Children's Hospital at Westmad

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