Expired Study
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Cambridge, Massachusetts 02138


Purpose:

The purpose of this study is to investigate the effectiveness of a medication skin patch called Methylphenidate Transdermal System (MTS). We will compare the MTS medicated patch to a placebo patch. We want to find out how well it treats ADHD during the early morning hours before a child leaves for school or summertime routines.


Criteria:

Inclusion Criteria: - Male and female outpatients 6 to 12 years of age. - Diagnosis of Attention Deficit Hyperactivity Disorder (ADHD), by DSM-IV, as manifested in clinical evaluation and confirmed by structured interview. - Participation in structured morning routine (e.g. school, camp, or other organized activities). Exclusion Criteria: - Mental retardation (IQ <75). - Subjects with a medical condition, or treatment that will either jeopardize subject safety or affect the scientific merit of the study. - Subjects with moderate to severe dermatological atopy. - Subjects with known structural cardiac abnormalities. - Organic brain disorders. - Seizure Disorder. - Subjects with Tourette's syndrome, or a history of psychosis or bipolar disorder. - Subjects with current comorbid psychopathology that in the investigator's opinion will warrant immediate treatment or will interfere with the safe execution of the protocol (i.e. Anxiety or Major Depressive Disorder rated as moderate on CGI). - Subjects with a history of intolerable adverse effects or non-response to methylphenidate. - Pregnant or nursing females.


NCT ID:

NCT00586157


Primary Contact:

Principal Investigator
Timothy Wilens, MD
Massachusetts General Hospital


Backup Contact:

N/A


Location Contact:

Cambridge, Massachusetts 02138
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 19, 2018

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