Status:
COMPLETED
Effect of Vyvanse on Sleep in Children Aged 6-12 Years With Attention Deficit Hyperactivity Disorder (ADHD)
Lead Sponsor:
Clinical Study Centers, LLC
Collaborating Sponsors:
Shire
Conditions:
Attention Deficit Hyperactivity Disorder
Sleep
Eligibility:
All Genders
6-12 years
Phase:
NA
Brief Summary
This study involves research to test how Vyvanse (study drug) affects sleep in 24 children aged 6 to 12 years who have ADHD. Vyvanse is approved by the FDA for the treatment ADHD of in children aged 6...
Detailed Description
Treatment with psychostimulants has been associated with sleep disturbances, including both sleep onset and maintenance problems, in children with ADHD. This analysis evaluated the effect of lisdexamf...
Eligibility Criteria
Inclusion
- Male or female subject 6 to 12 years of age, inclusive
- Subject meets DSM-IV-TR criteria for a primary diagnosis of ADHD
- Female subjects of childbearing potential (FOCP) must have a negative urine pregnancy test
- Subject must be in general good health
- Subject's parent or legally authorized guardian provides signature of informed consent, and there is documentation of assent by the subject.
- Subject and parent/caregiver are willing and able to comply with all the testing and requirements defined in the protocol.
- Subject is generally functioning academically at age-appropriate levels
- Subject is able to swallow a capsule.
- Subject and parent/guardian are willing to comply with entire visit schedule for the study and Sleep Hygiene Instructions
Exclusion
- Subject has a comorbid psychiatric diagnosis that contraindicates VyvanseTM treatment or would confound efficacy or safety assessments.
- Subject has any comorbid illness that could interfere with participation in the study.
- Subject is a known non-responder to an adequate trial of stimulant medication for ADHD.
- Subject has history of symptoms or has an identified sleep disorder
- Subject has a history of seizure during the last 2 years
- Subject is significantly overweight or obese
- Subject has any clinically significant ECG or laboratory abnormalities at screening or baseline.
- Subject has any specific cardiac condition or family history of cardiac disease
- Subject is taking medications that affect blood pressure or heart rate (except current ADHD therapy, if any).
- Subject has a positive urine drug result at screening (except current ADHD therapy, if any).
- Subject is hypertensive.
- Subject has any documented adverse reactions, allergy, or intolerance to amphetamines or dextroamphetamines.
- Subject is taking exclusionary medications
- Subject currently has (or had a history in the previous 12 months) a drug dependence or substance abuse disorder
- Subject has taken another investigational product or taken part in a clinical trial within the 30 days prior to Screening (Visit 1).
Key Trial Info
Start Date :
April 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2008
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT00807222
Start Date
April 1 2008
End Date
August 1 2008
Last Update
December 11 2008
Active Locations (1)
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1
Clinical Study Centers, LLC
Little Rock, Arkansas, United States, 72205