drugset / Trial / NCT00216918

Neuropsychological Functioning in Children With Attention-Deficit/Hyperactivity Disorder.

NCT00216918

Phase 4 Completed 40 enrolled Eli Lilly and Company
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the change in neuropsychological status from baseline to 6 months post-initiation of atomoxetine treatment in children ages 6 to 10.5 diagnosed with ADHD.

Timeline

Start
2005-09
Primary completion
Completion
2006-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Atomoxetine Other / unclassified