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
| Type | Name | Description |
|---|---|---|
| DRUG | Atomoxetine | |
| DRUG | Placebo |
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.