Skip to content

Desmopressin Monotherapy for Monosymptomatic Nocturnal Enuresis

Predictors of Success and Relapse After Desmopressin Monotherapy for Monosymptomatic Nocturnal Enuresis

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06285006
Enrollment
50
Registered
2024-02-29
Start date
2024-02-23
Completion date
2024-05-12
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nocturnal Enuresis

Keywords

Nocturnal enuresis, Desmopressin, Monotherapy

Brief summary

Nocturnal Enuresis (NE) is defined as the involuntary passage of urine during sleep past the age of usual control, which is considered a developmental age of 5 to 7 years. NE is a common problem that causes distress to both children and their families. It has an adverse impact on behavior and social life, affects self-esteem, and can result in poor emotional well-being. In Egypt, the prevalence of NE in primary school children is about 15.4%. The family history was seen to have had a markedly significant impact on the occurrence of NE in the studied children. The mainstay of treatment is urotherapy with information and psychoeducation about normal lower urinary tract function, the underlying cause of MNE, disturbed bladder dysfunction in the child with NMNE, and instructions about therapeutic strategies. Alarm therapy and desmopressin are effective in randomized trials. Children with NMNE first need treatment of the underlying daytime functional bladder problem before treatment of nocturnal enuresis.

Interventions

DRUGDesmopressin

Desmopressin is a synthetic analogue of ADH released by the posterior pituitary gland that reduces urine production by increasing water reabsorption by the collecting tubules.

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* School age group (from 7 to 14 years) * Primary monosymptomatic nocturnal enuresis

Exclusion criteria

Patients with one or more of the following will be excluded from the study. * Diurnal enuresis * Urinary tract infection within the preceding 3 months * Diabetes mellitus * History of renal disease, hypertension or genitourinary abnormality, neurological disease, or psychological disease. * Post-micturition residual urine \>1/3 expected bladder capacity. * Each patient will be subjected to the following.

Design outcomes

Primary

MeasureTime frameDescription
The number of episodes per week after desmopressin treatmentAfter the end of the treatment for one month.Patients will be evaluate by no. of episodes per week after desmopressin treatment.

Countries

Egypt

Contacts

Primary ContactOmnia Nassar, Dr
omnianassar835@gmail.com01010112054
Backup ContactHosny Elmasry, Prof
omnianassar835@gmail.com01010112054

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026