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临床试验/NCT07028645
NCT07028645进行中(未招募)不适用

Is Uroflowmetry Useful in Assessing Response to Pharmacological Treatment in Enuresis

Furkan Adem Canbaz1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年8月20日最近更新:
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
100
试验地点
1
主要终点
Number of days without bedwetting

研究概览

简要总结

This study will evaluate the uroflowmetry parameters of patients which were treated for enuresis.

详细描述

A total of approximately 100 patients with enuresis will be evaluated retrospectively. Uroflowmetry parameters of these patients will be evaluated. For this purpose, patients will be divided to mainly three groups according to the treatment choices.

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

  • Presence of enuresis nocturna
  • Patients who have uroflowmetry test

排除标准

  • Presence of lower urinary tract symptoms
  • Presence of anatomical or neurological problems
  • Patients with missing data

研究组 & 干预措施

Desmopressin 120mcg

Patients treated with desmopressin 120 mcg

干预措施: desmopressin melt form 120 μg (Drug)

Desmopressin 240 mcg

Patients treated with desmopressin 240mcg

干预措施: Desmopressin lyophilisate (Melt) (Drug)

Desmopressin 240 mcg + anticholinergic

Patients treated with desmopressin 240mcg + anticholinergic agent

干预措施: Propiverine tablet (Drug)

结局指标

主要结局

Number of days without bedwetting

时间窗: 1 month

Achievement of bedwetting in one or less night of a month

次要结局

未报告次要终点

研究者

发起方
Furkan Adem Canbaz
申办方类型
Other
责任方
Sponsor 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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