跳至主要内容
临床试验/NL-OMON28659
NL-OMON28659招募中不适用

The use of a Polycaprolactone Based Bulking Agent for the Treatment of Female Stress Urinary Incontinence.

AQLANE Medical BV.Yalelaan 1, 3584 CL UtrechtThe Netherlands0 个研究点目标入组 50 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
招募中
发起方
入组人数
50

研究概览

简要总结

ot applicable

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Subjects 18 years of age or older
  • 2. Subjects with predominant SUI as determined by the Questionnaire for Urinary Incontinence Diagnosis (QUID); Total Stress Score (Sum Q1-Q3) of > or equal to 4 and Total Urge Score (Sum Q1-Q6) of < 6.

排除标准

  • 1. Subjects who have received previous bulking agent implantation in the submucosa of the urethra or had any form of surgery to treat SUI.
  • 2. Subjects with any form of urinary incontinence other than predominant SUI.

研究者

发起方
AQLANE Medical BV.Yalelaan 1, 3584 CL UtrechtThe Netherlands

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