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临床试验/JPRN-UMIN000022613
JPRN-UMIN000022613已完成未知

Efficacy of mirabegron for voiding disorders in patient who underwent prostate low-dose-rate brachytherapy - Efficacy of mirabegron in patient treathed with brachytherapy

ara Medical University Department of Urology0 个研究点目标入组 218 人开始时间: 2016年7月1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
218

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 85years-old(—)
性别
Male

入选标准

  • 未提供

排除标准

  • considered unsuitable for the trial by doctors residual urine volume greater than 100 ml Qmax less than 5 ml per second contraindicated to medication with mirabegron history of urinary retention performance of clean intermittent catheterization

研究者

发起方
ara Medical University Department of Urology

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