跳至主要内容
临床试验/JPRN-UMIN000010327
JPRN-UMIN000010327招募中未知

Good combination therapy with alpha-blocker plus imidafenacin or mirabegron for nocturia in overactive bladder with benign prostatic hyperplasia; prospective randomized trial - Good-Night study 2

Osaka-Hokuriku maleLUTS Conference0 个研究点目标入组 300 人开始时间: 2013年3月27日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
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
20years-old 至 ot applicable(—)
性别
Male

入选标准

  • 未提供

排除标准

  • 1) Urinary retention within a year 2) Residual urine >=50mL 3) Strong suspect of prostate cancer 4) Treatment of any anti-muscarinic agent or beta-stimulants within a month. 5) Indwelling catheter or self intermittent urinary catherization 6) Diseases that affect nocturia (sleep apnea syndrome, restless legs syndrome, insomnia etc.) 7) The shift work, circadian rhythm disorder, and irregular lifestyle 8) Bladder training conducted over the past 10 days 9) Active acute urinary tract infection 10) Hormones or 5 alpha-reductase inhibitor started to have within the past six months 11) Contraindication to imidafenacin (primary angle-closure glaucoma, urinary retention, obstructive intestinal disease, paralytic ileus, gastrointestinal atony, myastania gravis) 12) Contraindication to mirabegron (severe heart disease, severe liver dysfunction, treatment of flecainide or propaphenone) 13) Untreated severe hypertension (more than Class II in JSH 2009, SBP>=160mmHg or DBP>= 100mmHg) 14) Judged as being unsuitable for the trial by physician.

研究者

发起方
Osaka-Hokuriku maleLUTS Conference

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