跳至主要内容
临床试验/JPRN-UMIN000011677
JPRN-UMIN000011677尚未招募未知

Comparison of efficacy and safety of the secondary treatment with increased fesoterodine and with mirabegron combination with 4mg fesoterodine for those who still have moderate or more overactive bladder symptoms after the initial treatment with 4mg fesoterodine: preliminary study - Comparison of efficacy and safety between increased fesoterodine and mirabegron combination for the overactive bladder resistant to the initial fesoterodine treatment.

Dept. of Urology, Otsu Minicipal Hospital0 个研究点目标入组 60 人开始时间: 2013年9月17日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
60

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 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients with the practice of catheterization past or present. 2) Residual urine volume is more than 100ml. 3) Patients who can`t urine voluntarily. 4) Neurogenic bladder, urethral stricture, urinary tract infection, urinary tract calculi, interstitial cystitis, chronic prostatitis, prostate cancer, bladder cancer 5) Patients who are contraindicated for fesoterodine administration. 6) Patients who are contraindicated for mirabegron administration. 7) Patients who have the history of the administration of contraindicated agents within 2 weeks.

研究者

发起方
Dept. of Urology, Otsu Minicipal Hospital

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