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临床试验/NCT04506697
NCT04506697Unknown不适用

Study of Remote Monitoring of Urination Dynamics

I.M. Sechenov First Moscow State Medical University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2020年3月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
30
试验地点
1
主要终点
Uroflowmetry during 24 hours

研究概览

简要总结

The aim of the study is to assess the possibility of using remote monitoring of urination.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •Men over 18 years old.
  • •The patient has performed uroflowmetry according to indications in the hospital no later than 7 days before the planned inclusion in the trial.
  • •Qmax = or <15 ml / sec.
  • •The patient has a smartphone (with Android 4.0 and higher, iOS 10.0 and higher) with Internet access

排除标准

  • •A patient with emergency conditions requiring surgical treatment
  • •Intellectual and cognitive abilities of the patient that do not allow him to follow the doctor's instructions and make it difficult to use the smartphone.

研究组 & 干预措施

Patients with LUTS

Experimental

Patients who are indicated for uroflowmetry

干预措施: Uroflowmetry (Procedure)

结局指标

主要结局

Uroflowmetry during 24 hours

时间窗: 1 day

Registration of remote uroflowmetry using portable uroflowmeter during 24 hours

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

Dmitry Enikeev, MD, PhD

Deputy Director for Research

I.M. Sechenov First Moscow State Medical University

研究点 (1)

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