36
Participants
Start Date
June 30, 2005
Primary Completion Date
December 31, 2008
Study Completion Date
June 30, 2009
atomoxetine
Patients will then be randomized (at Visit 2) to receive either atomoxetine or placebo for 4 weeks (Treatment Period); study drug will be titrated individually according to tolerability and efficacy (measured by ADHD-RS and CGI-I) completed at Visits 3, 4, 5, and 6) at 7-10 day intervals to a maximum dose of 1.8 mg/kg.
placebo
placebo
Rhode Island Hospital, Providence
Rhode Island Hospital
OTHER