The Effect of Guanfacine Extended-release on Attention Deficit Hyperactivity Disorder (ADHD)-Associated Insomnia

  • STATUS
    Recruiting
  • participants needed
    40
  • sponsor
    Children's Specialized Hospital
Updated on 8 November 2020
insomnia
polysomnography
actigraphy
initial insomnia

Summary

This study seeks to determine, using special sleep tests (polysomnography and actigraphy) if guanfacine extended release is able to improve nighttime sleep in children with ADHD - associated insomnia while improving daytime ADHD symptoms. Male and female children with diagnosed or suspected ADHD with sleep problems (difficulty falling asleep, difficulty staying asleep, or less than expected hours of sleep) will be recruited. After obtaining informed consent and assent (when appropriate) and after discontinuation of excluded medications, children will have evaluations of his or her sleep and evaluations confirming the ADHD diagnosis. Children who successfully pass screening will be enrolled into the double-blind, placebo-controlled, randomized investigation with 50% of participants receiving guanfacine extended release and 50% of participants receiving matching placebo. Using a flexible-dose optimization design based on ADHD symptom improvement and medication tolerability, the dose will be adjusted between 1 to 4 mg over the course of four weeks. At the end of medication adjustment (week 4 or 5), ADHD questionnaires, sleep questionnaires, and sleep tests will be repeated and analyzed. The medication will be weaned over the course of the following 3-10 days.

Details
Condition Attention Deficit Hyperactivity Disorder, Attention Deficit Disorder, Insomnia, Sleep Disorders
Treatment Placebo Comparator, Guanfacine extended-release tablets
Clinical Study IdentifierNCT01153178
SponsorChildren's Specialized Hospital
Last Modified on8 November 2020

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