MedPath

Remote Monitoring of Uroflowmetry

Not Applicable
Conditions
Lower Urinary Tract Symptoms
Interventions
Procedure: Uroflowmetry
Registration Number
NCT04506697
Lead Sponsor
I.M. Sechenov First Moscow State Medical University
Brief Summary

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

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
Male
Target Recruitment
30
Inclusion Criteria
  1. Men over 18 years old.
  2. The patient has performed uroflowmetry according to indications in the hospital no later than 7 days before the planned inclusion in the trial.
  3. Qmax = or <15 ml / sec.
  4. The patient has a smartphone (with Android 4.0 and higher, iOS 10.0 and higher) with Internet access
Exclusion Criteria
  1. A patient with emergency conditions requiring surgical treatment
  2. 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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Patients with LUTSUroflowmetryPatients who are indicated for uroflowmetry
Primary Outcome Measures
NameTimeMethod
Uroflowmetry during 24 hours1 day

Registration of remote uroflowmetry using portable uroflowmeter during 24 hours

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Institute for Urology and Reproductive Health, Sechenov University.

🇷🇺

Moscow, Russian Federation

© Copyright 2025. All Rights Reserved by MedPath