drugset / Trial / NCT06841666

Evaluating the Efficacy of Atomoxetine in Reducing Primary Nocturnal Enuresis in Children With ADHD: A Randomized, Placebo-Controlled Study

NCT06841666

Phase 0 Not yet recruiting 100 enrolled Tanta University
RandomizedParallel-groupOpen-labelHealth-services research

Summary

1. Primary Aim: To evaluate the efficacy of atomoxetine in reducing the frequency of primary nocturnal enuresis episodes in children with ADHD. 2. Secondary Aim: To determine if improvements in attention symptoms correlate with reductions in nocturnal enuresis episodes.

Timeline

Start
2025-02-28
Primary completion
2025-08-30
Completion
2025-09-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Atomoxetine Other / unclassified 0.5 mg/kg
Subject Atomoxetine Other / unclassified 1.2 mg/kg