Abstract
The efficacy and tolerability of osmotic-release oral system (OROS) methylphenidate in adolescents with attention deficit hyperactivity disorder (ADHD) were evaluated in a multisite controlled study at the Massachusetts General Hospital, Boston, and other centers in the United States.
Highlights
The efficacy and tolerability of osmotic-release oral system (OROS) methylphenidate in adolescents with attention deficit hyperactivity disorder (ADHD) were evaluated in a multisite controlled study at the Massachusetts General Hospital, Boston, and other centers in the United States
Investigator, parent and patient report measures showed a significant reduction from baseline in ADHD symptoms in 52% of subjects treated with OROS compared to 31% of those receiving placebo
OROS methylphenidate is effective in 50% of adolescents with ADHD following a short-term trial, but larger doses than usual are required in more than one-third of patients
Summary
The efficacy and tolerability of osmotic-release oral system (OROS) methylphenidate in adolescents with attention deficit hyperactivity disorder (ADHD) were evaluated in a multisite controlled study at the Massachusetts General Hospital, Boston, and other centers in the United States. Of 220 adolescents who entered the study, 177 completed an initial dose titration phase and were randomized to receive 2 weeks' treatment with their individualized, effective and tolerated dosage (18, 36, 54, or 72 mg once daily) or placebo. Investigator, parent and patient report measures showed a significant reduction from baseline in ADHD symptoms in 52% of subjects treated with OROS compared to 31% of those receiving placebo.
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