Clinical Trials Directory

Trials / Completed

CompletedNCT00380692

Atomoxetine Versus Placebo for Symptoms of Attention-Deficit/Hyperactivity Disorder (ADHD) in Children and Adolescents With Autism Spectrum Disorder

A Randomized, Double-blind Comparison of Atomoxetine Hydrochloride and Placebo for Symptoms of Attention-Deficit/Hyperactivity Disorder in Children and Adolescents With Autism Spectrum Disorder

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
97 (actual)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
6 Years – 17 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether atomoxetine is effective in reducing ADHD (Attention Deficit/Hyperactivity Disorder) symptoms in children and adolescents with ASD (Autism Spectrum Disorder).

Conditions

Interventions

TypeNameDescription
DRUGAtomoxetine
DRUGPlacebo

Timeline

Start date
2006-10-01
Primary completion
2008-05-01
Completion
2008-10-01
First posted
2006-09-26
Last updated
2010-05-11
Results posted
2009-07-08

Locations

8 sites across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00380692. Inclusion in this directory is not an endorsement.