14
Participants
Start Date
April 30, 2007
Primary Completion Date
October 31, 2008
Study Completion Date
February 28, 2009
Daytrana (methylphenidate patch)
Subjects will be provided with a 7-day supply of medication at each study visit. The dose will be flexible and will be titrated based on effect and tolerability. Unless a subject is experiencing side effects, the dose will be increased if a 25% reduction in ADHD symptoms as determined by the WRAADDS is not obtained. A proposed dosing schedule is as follows: Week 1: 12.5 cm2, Week 2: 18.75 cm2, Week 3: 25 cm2, Week 4: 37.5 cm2. The dose may be decreased as needed for tolerability.
Medical University of South Carolina, Charleston
Collaborators (1)
Shire
INDUSTRY
Medical University of South Carolina
OTHER