NL-OMON46734已完成4 期
Evaluation of the patients* satisfaction and safety of a non-degradable urethral bulking agent for female stress urinary incontinence - Euro study
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 75
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •- > 18 years
- •- who underwent treatment with bulkinjection therapy Urolastic for stress urinary incontinence
排除标准
- •Incapable of giving informed consent
研究者
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