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临床试验/NCT07046156
NCT07046156进行中(未招募)不适用

Evaluation of Anticholinergic Treatment Response and Predictive Factors in Pediatric Overactive Bladder

Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2022年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
120
试验地点
1
主要终点
Number of patients with drug related adverse effects

研究概览

简要总结

This study aims to evaluate the efficacy and adverse effect incidence of three different anticholinergics (oxybutinin, propiverine, and tolterodine) that are used in children with overactive bladder.

详细描述

A total of approximately 150 patients with overactive bladder will be evaluated retrospectively. Clinical and demographic data and voiding diaries of these patients will be evaluated. For this purpose, patients will be divided into mainly three groups according to the anticholinergic agent used.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
5 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Patients diagnosed with overactive bladder
  • Patients treated with an anticholinergic

排除标准

  • Presence of anatomical or neurological problems
  • Patients with missing data

研究组 & 干预措施

Oxybutynin

Patients treated with oxybutynin

干预措施: Oxybutynin Cl (Drug)

Propiverine

Patients treated with propiverine

干预措施: propiverine (Drug)

Tolterodine

Patients treated with tolterodine

干预措施: Tolterodine (Drug)

结局指标

主要结局

Number of patients with drug related adverse effects

时间窗: 1 month

Number of patients treated with anticholinergic

时间窗: 6 months

次要结局

未报告次要终点

研究者

发起方
Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Furkan Adem Canbaz

Medical doctor

Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital

研究点 (1)

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