跳至主要内容
临床试验/NL-OMON34244
NL-OMON34244已完成不适用

A randomised controlled trail comparing the TVT-O® with the Ajust® as primary surgical treatment of female stress urinary incontinence. - TOAST

niversitair Medisch Centrum Utrecht0 个研究点目标入组 145 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
145

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
18 至 99(—)

入选标准

  • 1. Predominant stress urinary incontinence
  • 2. The stress urinary incontinence is confirmed during physical examination, stress test or urodynamic assessment.
  • 3. They have completed conservative treatment for their stress urinary incontinence, pelvic floor muscle training program

排除标准

  • 1. A post voiding bladder volume of more than 100 ml.
  • 2. History of anti-incontinence surgery
  • 3. Genital prolapse Stage 2 or more according to the POP-Q classification
  • 4. Patients desire for future pregnancy and childbirth
  • 5. Co-morbidity

研究者

发起方
niversitair Medisch Centrum Utrecht

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