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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TERMINATED
19 participants
OBSERVATIONAL
2006-07-31
2010-07-31
Brief Summary
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Detailed Description
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A chi-square test will be conducted to determine whether there is differential representation of SNAP 25 among therapeutic methylphenidate responders versus non-responders. Statistical comparison will be performed using a two-tailed test at the .05 level of significance.
Conditions
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Keywords
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
2. Patients must meet DSM-IV criteria for ADHD
3. Patients and parents/guardians must have a degree of understanding sufficient to be able to communicate suitably with the investigator and study coordinator
4. Patients must have tolerated the drug at therapeutic doses, but have shown a true lack of improvement in symptoms
5. Must have shown clinically significant superiority in improvement in ADHD symptoms on amphetamine relative to MPH.
Exclusion Criteria
2. Must not have a history of serious adverse reactions to methylphenidate
6 Years
ALL
Yes
Sponsors
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UBC Human Early Learning Partnership (HELP)
UNKNOWN
University of British Columbia
OTHER
Responsible Party
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Principal Investigators
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Margaret D. Weiss, MD, Ph.D
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Jim Kennedy, MD
Role: STUDY_DIRECTOR
University of British Columbia
Atilla Turgay, MD
Role: STUDY_DIRECTOR
British Columbia Children's & Women's Hospital
Locations
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Provincial ADHD Program, BC Children's & Women's Health Centre
Vancouver, British Columbia, Canada
Countries
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Other Identifiers
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H05-70410
Identifier Type: -
Identifier Source: org_study_id