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NCT05190601 Clinical Trial

Uroflowmetry in Children With Enuresis Nocturnal

Enuresis Clinical Trial

Official title:
How Valuable is Uroflowmetry in Children With Enuresis Nocturnal?

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05190601
Other study ID # 14.102021/1600
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2020
Est. completion date December 11, 2021

Study information
Verified date December 2021
Source Hisar Intercontinental Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Background: Enuresis nocturna is an important social and psychological problem in children. Uroflowmetry is an important test used to investigate lower urinary tract symptoms.. Objective:To evaluate the uroflowmetry (UFM) results of children with nocturnal enuresis (NE). Method: The uroflowmetry findings of healthy and visualized children without any urinary symptoms and who were prospectively admitted to the urology and pediatric surgery outpatient clinic with the complaint of Enuresis nocturna between January 2020 and July 2021 were compared. Information (anamnesis, physical examination, radiology results and laboratory tests) and uroflowmetry results of NE and healthy children included in the study were recorded.

Description:

SMale and Female,

Recruitment information / eligibility
Status Completed
Enrollment 180
Est. completion date December 11, 2021
Est. primary completion date July 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 16 Years
Eligibility Inclusion Criteria: Primer monosymptomatic enuresis nocturna Exclusion Criteria: Urinary infectious Diabetes Spina bifida, Epispadias, Hipospadias VUR Extrophia Vesica Epilepsy Cerebral Palsy

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• uroflowmetry
Qmax(ml/s),Qav(ml/s),Volume (ml)

Locations
Country Name City State
Turkey Hisar Intercontinental Hospital Istanbul

Sponsors (1)
Lead Sponsor Collaborator
Hisar Intercontinental Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary uroflowmetry ml/s 2 years
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