View Clinical Trial (Medical Research Study)


Effectiveness of ATMX in Treating Adolescents With ADHD and SUD - NCT00218322-02114(Clinical Trial 130796)



ClinicalConnection.com has recently undergone an update and this page may no longer be up-to-date. Please Search For Clinical Trials to view the most current clinical trials listings.


Signup

City:  Boston
State:  
MA
Zip Code: 02114
Conditions: Attention Deficit Disorder With Hyperactivity - Substance-Related Disorders
Purpose: Adolescents with attention deficit hyperactivity disorder (ADHD) often develop substance use disorders (SUD). The purpose of this study is to evaluate the effectiveness of atomoxetine in treating adolescents dually diagnosed with ADHD and SUD.
Study summary: High rates of ADHD have been reported in adolescents with SUD. In addition, untreated ADHD is a risk factor for developing SUD. Atomoxetine is a norepinephrine reuptake inhibitor, and is currently used to treat adolescents with ADHD. The purpose of this trial is to evaluate the efficacy of atomoxetine in treating adolescents dually diagnosed with ADHD and SUD. This study will last up to 18 weeks. Participants will receive six treatments of manual-driven, cognitive behavioral therapy for substance abuse over at 6 or earlier weeks. Participants and their parents will partake in therapy sessions. Subjects who have completed at least 2 weeks of CBT will be eligible to enter the controlled trial, at which point participants will be randomly assigned to receive either atomoxetine or placebo, which they will take once daily for 12 weeks. At the Week 12 study visit, participants will be assessed for symptoms of ADHD and SUD.
Criteria: Inclusion Criteria: - DSM-IV diagnosis of ADHD - Current or recent (within the three months prior to study entry) SUD, including marijuana and alcohol abuse - ADHD CGI-S score of greater to or equal to 4 Exclusion Criteria: - Any Unstable medical condition - Recent history of intravenous drug use or cocaine dependence - Currently abusing ecstasy, cocaine, gamma-hydroxybutyrate, methamphetamine, amphetamine, opioids, phencyclidine, or benzodiazepine - Mental retardation or organic brain syndrome - Currently psychotic or history of bipolar disorder - Currently taking any psychotropic or anti-substance abuse disorder medications - Current DSM-IV diagnosis of major depression, depressive disorder, or anorexia - Pregnant or breastfeeding
Study is available at: Massachusetts General Hospital
Boston, MA 02114
United States

Primary Contact:
Kerry V. Brodziak, BA
Email: kbrodziak@partners.org
Phone: 617-503-1043

Secondary Contact:
Kerry V. Brodziak, BA
Email: kbrodziak@partners.org
Phone: 617-503-1043
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
Trials Alerts: If you would like to be notified of new clinical trials as they become available please register for a free account.

Data Source: ClinicalTrials.gov
Date Processed: March 21, 2011
Modifications to
this listing:
Only selected fields are shown, please use the link above to view all information about this clinical trial.