JPRN-jRCT2080221272未知3 期
A phase III parallel-group comparison study of HOB-294 in patients with overactive bladder.
适应症
试验速览
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
- ot applicable 至 ot applicable（—）
- 性别
- All
入选标准
- •Patients with symptoms of overactive bladder for at least 24 weeks before obtaining informed consent
排除标准
- •- Patients with genuine stress incontinence
- •- Patients with micturition difficulty, retention of urine, or other symptoms due to lower urinary tract obstruction
- •- Patients for whom it is difficult to walk to the lavatory without assistance, patients who cannot measure the urine volume by themselves, and patients who cannot keep a bladder log by themselves
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