Psychomotor functioning and alertness with guanfacine extended release in subjects with attention-deficit/hyperactivity disorder

To determine whether treatment with guanfacine extended release (GXR) in subjects with attention-deficit/hyperactivity disorder (ADHD) disrupted psychomotor functioning and alertness, or impacted daytime sleepiness. This was a randomized, double-blind, placebo-controlled, multicenter, phase 2, dose-...

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Veröffentlicht in:Journal of child and adolescent psychopharmacology 2011-04, Vol.21 (2), p.111-120
Hauptverfasser: Kollins, Scott H, López, Frank A, Vince, Bradley D, Turnbow, John M, Farrand, Kimberly, Lyne, Andrew, Wigal, Sharon B, Roth, Thomas
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container_end_page 120
container_issue 2
container_start_page 111
container_title Journal of child and adolescent psychopharmacology
container_volume 21
creator Kollins, Scott H
López, Frank A
Vince, Bradley D
Turnbow, John M
Farrand, Kimberly
Lyne, Andrew
Wigal, Sharon B
Roth, Thomas
description To determine whether treatment with guanfacine extended release (GXR) in subjects with attention-deficit/hyperactivity disorder (ADHD) disrupted psychomotor functioning and alertness, or impacted daytime sleepiness. This was a randomized, double-blind, placebo-controlled, multicenter, phase 2, dose-optimization, noninferiority, laboratory classroom study of GXR (1, 2, and 3 mg/day) in 182 subjects aged 6 to 17 years with ADHD. Psychomotor functioning and alertness were assessed through several measures, including the Choice Reaction Time (CRT) test from the Cambridge Neuropsychological Test Automated Battery. Sedative effects were examined via spontaneously reported adverse events of sedation, somnolence, and hypersomnia as well as fatigue and lethargy, and with two validated subject- and observer-rated sleepiness scales. Standard efficacy measures for ADHD also were included. Cardiovascular and laboratory parameters were assessed. There were no significant differences between the GXR and placebo groups on measures of psychomotor functioning or alertness from the CRT at endpoint (least-square mean difference: 2.5 [95% confidence interval (CI): -22.9, 28.0], p = 0.8 for CRT; 2.5 [95% CI: -21.5, 26.4], p = 0.84 for correct responses; 15.5 [95% CI: -45.1, 14.1], p = 0.30 for movement time; and -8.2 [95% CI: -54.1, 37.6] p = 0.72 for total time). Most sedative adverse events were mild to moderate, occurred during dose titration, decreased with dose maintenance, and resolved during the study period. One subject in the GXR group discontinued due to fatigue and somnolence. GXR was not associated with increased daytime sleepiness. GXR treatment was associated with significant improvement in ADHD symptoms (6.3 [95% CI: 2.7, 9.8], p = 0.001 for ADHD Rating Scale IV total scores at endpoint). At doses that resulted in significant improvement in ADHD symptoms, impairment on cognitive tasks was not observed. Daytime sleepiness did not differ with GXR compared with placebo. Results suggest that the beneficial effects of GXR on ADHD symptoms are independent of sedation.
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Daytime sleepiness did not differ with GXR compared with placebo. 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This was a randomized, double-blind, placebo-controlled, multicenter, phase 2, dose-optimization, noninferiority, laboratory classroom study of GXR (1, 2, and 3 mg/day) in 182 subjects aged 6 to 17 years with ADHD. Psychomotor functioning and alertness were assessed through several measures, including the Choice Reaction Time (CRT) test from the Cambridge Neuropsychological Test Automated Battery. Sedative effects were examined via spontaneously reported adverse events of sedation, somnolence, and hypersomnia as well as fatigue and lethargy, and with two validated subject- and observer-rated sleepiness scales. Standard efficacy measures for ADHD also were included. Cardiovascular and laboratory parameters were assessed. 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subjects Adolescent
Adrenergic alpha-2 Receptor Agonists - administration & dosage
Adrenergic alpha-2 Receptor Agonists - adverse effects
Adrenergic alpha-2 Receptor Agonists - therapeutic use
Alertness (Psychology)
Attention Deficit Disorder with Hyperactivity - drug therapy
Attention Deficit Disorder with Hyperactivity - psychology
Attention deficit hyperactivity disorder
Child
Children & youth
Clinical trials
Delayed-Action Preparations
Disorders of Excessive Somnolence - chemically induced
Disorders of Excessive Somnolence - drug therapy
Dosage and administration
Dose-Response Relationship, Drug
Double-Blind Method
Drug Administration Schedule
Drug therapy
Evaluation
Fatigue - chemically induced
Fatigue - drug therapy
Female
Guanfacine
Guanfacine - administration & dosage
Guanfacine - adverse effects
Guanfacine - therapeutic use
Humans
Male
Patient outcomes
Placebos
Psychiatric Status Rating Scales
Psychomotor Performance - drug effects
Treatment Outcome
title Psychomotor functioning and alertness with guanfacine extended release in subjects with attention-deficit/hyperactivity disorder
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