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临床试验/NCT02130375
NCT02130375已完成4 期

Clinical and Urodynamic Effects of Minimally Laser (IncontiLaseTM) Procedure for Female Stress Urinary Incontinence

National Taiwan University Hospital2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2014年5月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
35
试验地点
2
主要终点
The change of pad weight from baseline

研究概览

简要总结

The purpose of this study is to get the effect of IncontiLaseTM procedure; and its impact on urinary symptoms and female sexual function.

详细描述

To get the objective urodynamic and sonographic effects of IncontiLaseTM procedure on women with stress urinary incontinence; and its impact on urinary symptoms and female sexual function.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 99 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • All consecutive sexually active and parous adult women with the complaint of stress urinary incontinence

排除标准

  • < 20 years old female

结局指标

主要结局

The change of pad weight from baseline

时间窗: 3 months

The change of pad weight from baseline after IncontiLaseTM procedure

次要结局

  • The change of maximum urethral closure procedure from baseline(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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