跳至主要内容
临床试验/CTIS2023-510280-35-00
CTIS2023-510280-35-00
招募中
1 期

Effective strategy of withdrawal of pharmacological treatment of urinary incontinence in children (StayDry) - StayDry-2023

Region Midtjylland0 个研究点目标入组 216 人2024年1月9日

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
Daytime urinary incontinence
发起方
Region Midtjylland
入组人数
216
状态
招募中
最后更新
去年

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2024年1月9日
结束日期
待定
最后更新
去年
研究类型
Interventional clinical trial of medicinal product
性别
All

研究者

发起方
Region Midtjylland

入排标准

入选标准

  • The participants custody holder(s) must voluntarily sign and date an informed consent prior to initiation any study specific procedures., Age 5 to 14 years (inclusive) at the time of signing the consent., Diagnose with urinary incontinence as per ICCS criteria., Pharmacological treatment with solifenacin and/or mirabegron., Continence has been achieved on pharmacological therapy with solifenacin and/or mirabegron., Previously withdrawal attempts are accepted., Continence remained on the same dosage of medication for a minimum of three months.

排除标准

  • Neurogenic detrusor overactivity (neurogenic bladder)

结局指标

主要结局

未指定

相似试验