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 人开始时间: 2024年1月9日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
216

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

年龄范围
0 至 17(—)
性别
All

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)

研究者

发起方
Region Midtjylland

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