DRUG
Fluoxetine 20 MG
fluoxetine
Status
Unknown
Phase
Not applicable
Enrollment
60
Locations
1
Results
Not posted
Publications
0
Study summary
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
DRUG
fluoxetine
DRUG
desmopressin
Timeline
First posted
Dec 29, 2023
Study start
Dec 1, 2022
Primary completion
Mar 1, 2024
Study completion
Mar 1, 2024
Results posted
Not reported
Registry updated
Dec 29, 2023
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)
Not reported in the indexed record.
Eligibility
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
Egypt. Showing up to 24 locations stored in the fast local snapshot.
Faculty of medicine, Fayoum University
Al Fayyum, Egypt
Publications
No PMID-linked publications were present in this registry snapshot.
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