Phase
Condition
Attention Deficit/hyperactivity Disorder (Adhd - Adults)
Autism
Asperger's Disorder
Treatment
Randomization to either Alpha 2 agonist class of medication or alternate class of stimulant.
Randomization to either Amphetamine (AMP) class of stimulant medication or Methylphenidate (MPH) class of stimulant medication
Clinical Study ID
Ages 4-17 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Participant and/or legal caregiver must be willing and able to give informedconsent/assent for participation in this study.
Participant and/or legal caregiver must be willing and able (in the Investigator'sopinion) to comply with all study requirements.
Participant must be between 4 and 17 years of age (inclusive) at time of enrollment.
Participant must have a confirmed diagnosis of ASD based on supportive evidence (e.g. referring physician's report, medical records, such as ADOS or CARS, etc.).
Participant must have the ability to consistently take medication (via pill, liquidor mixed with food/liquid).
Participant must have a confirmed diagnosis of ADHD (based upon DSM-5 criteria andsupportive evidence).
Participant must have a consistent reporter (e.g., parent) who spends regular timewith the child.
Participant can be on other psychotropic medications (selective serotonin reuptakeinhibitor (SSRI), atypical antipsychotic, anticonvulsant) if dose has been stablefor > 4 weeks prior to consent with no plans for a dose change during the study.
It has been at least 7 days since the participant last took an ADHD medication andthe presiding clinician believes this to be a sufficient amount of time.
Caregiver must be sufficiently fluent in English or Spanish to be able to completequestionnaires relevant to this study.
Exclusion
Exclusion Criteria:
Participant has taken ADHD medication within the past 7 days.
Participant is not stable on other medications (< 4 weeks).
Any other risk factor that might prevent patient from safely taking the studymedications.
- There are no inclusion/exclusion criteria based upon participant IQ. We willinclude individuals across the entire range of cognition, just as practitionersare asked to treat ADHD in children with ASD across the entire IQ range.
Study Design
Study Description
Connect with a study center
University of Alberta, Glenrose Rehabilitation Hospital
Edmonton,
CanadaActive - Recruiting
Holland Bloorview Kids Rehabilitation Hospital
Toronto,
CanadaActive - Recruiting
University of California, Irvine
Irvine, California 92697
United StatesActive - Recruiting
Children's Hospital Los Angeles
Los Angeles, California 90027
United StatesActive - Recruiting
Maine Medical Center
Portland, Maine 04102
United StatesActive - Recruiting
Massachusetts General Hospital Lurie Center for Autism
Boston, Massachusetts 02421
United StatesActive - Recruiting
University of Rochester
Rochester, New York 14642
United StatesActive - Recruiting
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio 45229
United StatesActive - Recruiting
Nationwide Children's Hospital
Columbus, Ohio 43205
United StatesActive - Recruiting
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania 19178
United StatesActive - Recruiting
University of Pittsburgh
Pittsburgh, Pennsylvania 15262
United StatesActive - Recruiting
University of Virginia
Charlottesville, Virginia 22903
United StatesActive - Recruiting
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