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NOT YET RECRUITING
NCT07776977
NA

Bedtime Device Restriction and Desmopressin in PMNE.

Sponsor: Al-Azhar University

View on ClinicalTrials.gov

Summary

This randomized controlled trial will evaluate whether restricting bedtime digital-device use improves the response to desmopressin in children with primary monosymptomatic nocturnal enuresis. Participants will receive desmopressin for 8 weeks and will be assigned to either bedtime device restriction or usual screen habits.

Official title: Effect of Bedtime Digital-Device Restriction on the Therapeutic Response to Desmopressin in Children With Primary Monosymptomatic Nocturnal Enuresis: A Randomized Controlled Trial

Key Details

Gender

All

Age Range

6 Years - 14 Years

Study Type

INTERVENTIONAL

Enrollment

140

Start Date

2026-08

Completion Date

2027-07

Last Updated

2026-08-20

Healthy Volunteers

No

Interventions

DRUG

Desmopressin

Oral desmopressin administered at bedtime for 8 weeks for treatment of primary monosymptomatic nocturnal enuresis.

BEHAVIORAL

Bedtime digital-device restriction

Restriction of digital-device use, including smartphones, tablets, televisions, computers, and video games, for at least 60 minutes before habitual bedtime during the 8-week treatment period.

Locations (1)

Department of Urology, Al-Hussein and Sayed Galal University Hospitals, Al-Azhar University

Cairo, Egypt