Current partner codePEPTIDESDE
NCT06285006·Not applicable·INTERVENTIONAL

Desmopressin Monotherapy for Monosymptomatic Nocturnal Enuresis

Status

Unknown

Phase

Not applicable

Enrollment

50

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

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

Treatment arms and agents.

DRUG

Desmopressin

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.

Timeline

From registration to results.

  1. First posted

    Feb 29, 2024

  2. Study start

    Feb 23, 2024

  3. Primary completion

    May 1, 2024

  4. Study completion

    May 12, 2024

  5. Results posted

    Not reported

  6. Registry updated

    Apr 23, 2024

Outcomes

What the study measures.

Primary outcomes

The number of episodes per week after desmopressin treatment

Time frame · After the end of the treatment for one month.

Patients will be evaluate by no. of episodes per week after desmopressin treatment.

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
7 Years
Maximum age
14 Years
Sex
ALL
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.

Study locations

1 registered sites.

Egypt. Showing up to 24 locations stored in the fast local snapshot.

Alazhar university

Asyut, Egypt

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Desmopressin.

Related PeptideStat pages

Put the record in context.

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