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临床试验/NCT07149532
NCT07149532已完成不适用

Standard Urotherapy for Dysfunctional Voiding in Children: A Randomized Clinical Study

Tanta University1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2025年2月26日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
140
试验地点
1
主要终点
Overall response rate

研究概览

简要总结

This study aims to assess the efficiency of the standard urotherapy for the management of dysfunctional voiding in children.

详细描述

Dysfunctional voiding (DV) in children may result in lower urinary tract symptoms (LUTS), such as urgency, frequency, urinary incontinence, and difficulty in urination.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Children less than 18 years old.
  • Both sexes.
  • Children with dysfunctional voiding.

排除标准

  • Patients with cognitive function impairment.
  • Patients who received any care for dysfunctional voiding.
  • Children with known anatomical anomalies of the urinary tract.
  • Children with known neurological anomalies (spinal dysraphism, multiple sclerosis, lumbar or spinal neuritis……… etc).
  • Children with a history of back or lower urinary tract trauma.

研究组 & 干预措施

Group 1

Active Comparator

Patients will receive the standard urotherapy (SUT) .

干预措施: Standard urotherapy (SUT) alone. (Behavioral)

Group 2

Sham Comparator

Patients will receive nothing

干预措施: Sham control (Other)

结局指标

主要结局

Overall response rate

时间窗: 6 months post-procedure

Overall response rate will be recorded.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohamed Ibrahim Ahmed Elmaadawy

Lecturer of Urology, Faculty of Medicine, Tanta University, Tanta, Egypt.

Tanta University

研究点 (1)

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