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临床试验/NCT03267719
NCT03267719已完成不适用

Intravaginal Laser Treatment of Mild and Moderate Stress Incontinence

University Hospital Tuebingen2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2017年8月31日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
Quality of life

研究概览

简要总结

The aim of the study is to evaluate the effectiveness of laser therapy as a non-surgical treatment option in patients with mild and moderate stress incontinence.

详细描述

The aim of the study is to evaluate the effectiveness of laser therapy as a non-surgical treatment option in patients with mild and moderate stress incontinence.

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
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Light or moderate stress incontinence
  • mixed urine incontinence with predominance of the stress component
  • written informed consent

排除标准

  • Pregnancy
  • patients treated radiotherapy in the small basin
  • connective tissue disorders (e.g., Ehlers-Danlos syndrome, Marfan syndrome)
  • patient with or after malignant disease of the uterus, ovaries, vagina and vulva
  • former surgery due to stress incontinence (except for the patients who had a TVT insert with removal of the TVT)
  • Descensus genitalis> POPQ Stage 1
  • former surgery due to a genital lowering with vaginal netting

结局指标

主要结局

Quality of life

时间窗: 6 month

Quality of life will be access via ICIQ-SF questionaire

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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