Study Results
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View full resultsBasic Information
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COMPLETED
EARLY_PHASE1
138 participants
INTERVENTIONAL
2020-11-01
2024-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
QUADRUPLE
Study Groups
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Placebo Then Methamphetamine
Participants first receive placebo at their first session in the laboratory. Then will return to the laboratory 72 hours later and will receive 20 mg methamphetamine.
Methamphetamine
Participants will be given 20 mg of Methamphetamine.
placebo oral tablet
Participants will be given a placebo capsule that will only contain lactose.
MethamphetamineThen Placebo
Participants first receive 20 mg methamphetamine at their first session in the laboratory Then will return to the laboratory 72 hours later and will receive placebo.
Methamphetamine
Participants will be given 20 mg of Methamphetamine.
placebo oral tablet
Participants will be given a placebo capsule that will only contain lactose.
Interventions
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Methamphetamine
Participants will be given 20 mg of Methamphetamine.
placebo oral tablet
Participants will be given a placebo capsule that will only contain lactose.
Eligibility Criteria
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Inclusion Criteria
* Right Handed
* Less than 4 alcohol or caffeinated beverages a day.
Exclusion Criteria
* Any medical condition requiring regular medication
* Individuals with a current (within the last year) DSM-IV Axis 1 diagnosis
* Individuals with a history of dependence on stimulant drugs
* Women who are pregnant or trying to become pregnant.
18 Years
35 Years
ALL
Yes
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
University of Chicago
OTHER
Responsible Party
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Principal Investigators
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Harriet de Wit
Role: PRINCIPAL_INVESTIGATOR
Principal Investigator
Locations
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University of Chicago
Chicago, Illinois, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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IRB20-0364
Identifier Type: -
Identifier Source: org_study_id
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