Trials / Terminated
TerminatedNCT00687609
Pilot Evaluation of Atomoxetine on Attention Deficit Hyperactivity Disorder (ADHD) Symptoms in Adolescents With Cannabis abusE
An Open Label Pilot Study of Atomoxetine Hydrochloride in Adolescents With Attention Deficit/Hyperactivity Disorder and Comorbid Cannabis Abuse.
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 7 (actual)
- Sponsor
- Eli Lilly and Company · Industry
- Sex
- All
- Age
- 13 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 adolescents with ADHD and comorbid cannabis abuse.
Detailed description
In the past adolescents with cannabis abuse have been excluded from studies in which atomoxetine for ADHD symptoms was studied. In this study the efficacy of atomoxetine on symptoms of ADHD in adolescents with ADHD and comorbid cannabis abuse will be studied.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Atomoxetine | 0.5 milligrams per kilogram (mg/kg) daily for 1 week followed by 1.2 mg/kg daily for 11 weeks, orally, capsules. |
Timeline
- Start date
- 2008-09-01
- Primary completion
- 2009-06-01
- Completion
- 2009-06-01
- First posted
- 2008-06-02
- Last updated
- 2010-08-24
- Results posted
- 2010-08-19
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT00687609. Inclusion in this directory is not an endorsement.