NCT07508111

Brief Summary

Nocturnal enuresis, commonly known as bedwetting, is a frequent condition that affects many children and can have a significant impact on their self-esteem, social life, and family stress. The causes of bedwetting can vary widely, ranging from deep sleep patterns and excess nighttime urine production to underlying medical conditions like constipation, urinary tract infections, or enlarged tonsils and adenoids (which can affect breathing during sleep).The main goal of this descriptive study is to understand the different types and the underlying causes of bedwetting among children attending the pediatric outpatient clinics at Assiut University Children's Hospital. By identifying these specific causes in the local population, healthcare providers can offer better, more targeted treatments and help reduce the stigma surrounding this condition. During a single clinic visit, researchers will collect information through a structured interview with the parents and the child. The study involves a routine physical examination, including checking weight, height, and looking for physical signs of constipation or enlarged tonsils. Participants will also undergo standard tests to help pinpoint any medical causes, such as a urine test (urinalysis and culture), a basic ultrasound of the abdomen and pelvis, and potentially plain X-rays if issues like severe constipation or airway blockages are suspected. The study aims to include at least 80 male and female children aged 5 years and older who have been experiencing bedwetting at least twice a week for three months or more.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for all trials

Timeline
10mo left

Started May 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress24%
May 2026Jun 2027

First Submitted

Initial submission to the registry

March 27, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 2, 2026

Completed
29 days until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2027

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

April 2, 2026

Status Verified

March 1, 2026

Enrollment Period

1 year

First QC Date

March 27, 2026

Last Update Submit

March 27, 2026

Conditions

Keywords

Nocturnal EnuresisBedwettingUrinary IncontinencePediatricsPrimary EnuresisSecondary EnuresisMonosymptomatic Enuresis

Outcome Measures

Primary Outcomes (1)

  • Percentage of Participants with Identified Medical Causes for Nocturnal Enuresis

    The proportion of enrolled children diagnosed with underlying medical conditions contributing to nocturnal enuresis. This is determined through structured clinical history, physical examinations, and diagnostic investigations. Specific underlying factors evaluated include constipation (assessed using the Bristol Stool Scale and Rome IV criteria) , urinary tract infections (confirmed via urine culture) , and adenotonsillar hypertrophy (assessed using the Brodsky scale). The outcome will be reported as the percentage of the study cohort presenting with one or more of these identified medical conditions.

    Up to 7 days from the initial clinic visit

Study Arms (1)

Children with Nocturnal Enuresis

Male and female children over 5 years of age presenting with nocturnal enuresis (involuntary voiding during sleep ≥2 nights/week for ≥3 months) at the pediatric outpatient clinics at Assiut University Hospital. This observational cohort will be evaluated via clinical history, physical examination, and routine laboratory and imaging investigations. The purpose is to determine the prevalence, types (primary vs. secondary, mono vs. polysymptomatic), and associated causes (e.g., constipation, UTI, adenotonsillar hypertrophy, malformations) of their condition.

Eligibility Criteria

Age5 Years - 18 Years
Sexall
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of male and female children aged 5 years and older who present with nocturnal enuresis at the pediatric outpatient clinics of Assiut University Children's Hospital in Assiut, Egypt. For the purpose of this study, nocturnal enuresis is defined as involuntary voiding during sleep occurring at least twice a week for a duration of at least three months. The target population includes patients presenting with both primary and secondary enuresis, as well as mono-symptomatic and poly-symptomatic forms. Children with known neurological disorders (such as epilepsy or cerebral palsy), diabetes mellitus, acute urinary tract infections requiring immediate treatment, or structural anomalies of the urinary system requiring immediate surgery are excluded from this population.

You may qualify if:

  • Male and female children aged above 5 years.
  • Presenting with nocturnal enuresis, defined as involuntary voiding during sleep for ≥2 nights/week for ≥3 months.
  • Parents or caregivers providing informed consent, including child assent where applicable.

You may not qualify if:

  • Children with known neurological disorders, such as epilepsy or cerebral palsy.
  • Presence of an acute urinary tract infection (indicated by a positive urine culture requiring treatment).
  • Children diagnosed with diabetes mellitus.
  • Structural anomalies of the urinary system requiring immediate surgery, such as severe hypospadias.
  • Families unwilling to participate or complete follow-up data collection.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Nocturnal EnuresisUrinary Incontinence

Condition Hierarchy (Ancestors)

EnuresisUrination DisordersUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesBehavioral SymptomsBehaviorElimination DisordersMental DisordersLower Urinary Tract SymptomsUrological ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident at Pediatric Department, Assiut University

Study Record Dates

First Submitted

March 27, 2026

First Posted

April 2, 2026

Study Start

May 1, 2026

Primary Completion (Estimated)

May 1, 2027

Study Completion (Estimated)

June 1, 2027

Last Updated

April 2, 2026

Record last verified: 2026-03