Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
61 participants
OBSERVATIONAL
2011-04-30
2015-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
2. Subject must have a current DSM-IV diagnosis of high functioning ASD, based on past evaluations at the Bressler Clinic.
3. Subjects must have a level of understanding sufficient to communicate intelligently with the investigator and study coordinator, and to cooperate with all tests and examinations required by the protocol.
4. Each subject must understand the nature of the study. The subject must sign an IRB approved informed consent.
Exclusion Criteria
2. Contraindication to MRI including presence of metal or surgical devices (plates, implants, braces or other items).
3. Neuropsychiatric conditions (such as dementia) which sufficiently impair cognition such that a surrogate consent would be required.
4. Neurological disorders associated with gross brain pathology (other than atrophy), e.g., stroke, tumors, or demyelinating diseases.
5. Pregnancy.
13 Years
ALL
No
Sponsors
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Harvard University
OTHER
Massachusetts General Hospital
OTHER
Responsible Party
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Gagan Joshi
Clinical Investigator, Clinical and Research Program in Pediatric Psychopharmacology and Adult ADHD
Principal Investigators
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Gagan Joshi, MD
Role: PRINCIPAL_INVESTIGATOR
Massachusetts General Hospital
Locations
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Massachusetts General Hospital
Boston, Massachusetts, United States
Countries
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Other Identifiers
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2011P000375
Identifier Type: -
Identifier Source: org_study_id
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