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ABSTRACT: Objective
To evaluate the efficacy of lisdexamfetamine dimesylate in adults with attention deficit hyperactivity disorder symptom subtypes who exhibit predominantly inattention, hyperactivity/ impulsivity, or combined symptom clusters.Design/setting/participants
This is a post-hoc analysis from a multicenter, one-year, open-label lisdexamfetamine dimesylate study in adults with attention deficit hyperactivity disorder previously completing two weeks or more in a four-week, randomized, placebo-controlled lisdexamfetamine dimesylate study, using Attention Deficit Hyperactivity Disorder Rating Scale IV symptom ratings as an attention deficit hyperactivity disorder subtype proxy (N=349).Measurements
Attention Deficit Hyperactivity Disorder Rating Scale IV was measured a
SUBMITTER: Mattingly G
PROVIDER: S-EPMC3398683 | biostudies-literature | 2012 May
REPOSITORIES: biostudies-literature