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临床试验/JPRN-UMIN000024442
JPRN-UMIN000024442未知4 期

Comparison of fesoterodine and mirabegron in the treatment of female overactive baldder patients with urgency incontinence: A randomized, prospective study (Feminine study) - Feminine study

Department of urology, Nagoya University Graduate School of Medicine0 个研究点目标入组 300 人开始时间: 2016年11月1日最近更新:
适应症

试验速览

阶段
4 期
发起方
入组人数
300

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
50years-old 至 ot applicable(—)
性别
Female

入选标准

  • 未提供

排除标准

  • Patients were excluded if they received oral anticholinergic agents, alpha1-blockers, antidepressants, or anti-anxiety agents, had obvious neurogenic bladder dysfunction, bladder calculi, or active urinary tract infection, or had severe cardiac disease, renal dysfunction (serum-creatinine >2 mg/dL), and/or hepatic dysfunction (i.e., aspartate aminotransferase and alanine aminotransferase levels of more than twice the normal value)

研究者

发起方
Department of urology, Nagoya University Graduate School of Medicine

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