JPRN-UMIN000037890已完成未知
Prospective, single-center, randomized, single-blind sham-controlled study of the urinary dysfunction treatment device O-NES in patients with overactive bladder who are unresponsive to or unsuitable for conservative therapy (pilot study) - Prospective, single-center, randomized, single-blind sham-controlled study of the urinary dysfunction treatment device O-NES in patients with overactive bladder who are unresponsive to or unsuitable for conservative therapy (pilot study)
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 47
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.They have any implantable electronic device (e.g. pacemaker). 2.They have received electrical or magnetic stimulation therapy for an overactive bladder in the past. 3.They have a history of treatment with botulinum toxin for the bladder. 4.They have been diagnosed with severe stress urinary incontinence. 5.They have functional urinary incontinence. 6.They have infection or calculus of the lower urinary tract. 7.They have organic urinary tract obstruction. 8.They have been diagnosed with interstitial cystitis.
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