Ontology highlight
ABSTRACT: Objective
To evaluate the efficacy and safety of lisdexamfetamine dimesylate in participants with attention deficit hyperactivity disorder and a history of depression and/or substance use disorder. History of these comorbidities was recorded from medical history forms completed by the study clinicians.Design/setting
An exploratory, post-hoc analysis was conducted using data from a randomized, double-blind, placebo-controlled, forced-dose titration study of lisdexamfetamine dimesylate.Participants
Adults with attention deficit hyperactivity disorder.Measurements
Changes in Attention Deficit Hyperactivity Disorder Rating Scale IV total scores and Clinical Global Impressions-Improvement scale were used to evaluate the efficacy of lisdexamfetamine dimesylate. Th
SUBMITTER: Kollins SH
PROVIDER: S-EPMC3071091 | biostudies-literature | 2011 Feb
REPOSITORIES: biostudies-literature