Current partner codePEPTIDESDE
NCT06185361·Not applicable·INTERVENTIONAL

Selective Serotonin Reuptake Inhibitors, Fluoxetine Versus the Standard Oral Desmopressin for Management of Mono-symptomatic Nocturnal Enuresis.

Status

Unknown

Phase

Not applicable

Enrollment

60

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

To determine whether there is a role for the selective serotonin reuptake inhibitors fluoxetine versus desmopressin in the treatment of nocturnal enuresis in children who have not responded to standard nonpharmacological urotherapy, and whether there are side effects involved.

Interventions

Treatment arms and agents.

DRUG

Fluoxetine 20 MG

fluoxetine

DRUG

Desmopressin

desmopressin

Timeline

From registration to results.

  1. First posted

    Dec 29, 2023

  2. Study start

    Dec 1, 2022

  3. Primary completion

    Mar 1, 2024

  4. Study completion

    Mar 1, 2024

  5. Results posted

    Not reported

  6. Registry updated

    Dec 29, 2023

Outcomes

What the study measures.

Primary outcomes

The children will be non-responders, partial responders, or full responders to therapy

Time frame · three months

The standardization of terminology of lower urinary tract function in children and adolescents: Update report from the standardization committee of the International Children's Continence Society "ICCS definitions" (i.e., if the reduction of enuresis frequency was below or above 50% or 90%, respectively)

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
8 Years
Maximum age
16 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: 1. Age ≥ 7 years 2. Severe enuresis with at least (50%) seven wet nights out of 14 3. Failed treatment 4. The enuresis alarm was either ineffective or considered impractical due to the family circumstances. Exclusion Criteria: 1. Underlying renal, urologic, neurologic, endocrinologic, or cardiac conditions 2. Patients with psychiatric disorders and behavioral disorders including depression, attention-deficit/hyperactivity disorder. 3. Untreated constipation 4. Contraindications to fluoxetine or desmopressin treatment

Study locations

1 registered sites.

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

Faculty of medicine, Fayoum University

Al Fayyum, 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.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.