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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04642820
Other study ID # IRB20-0364
Secondary ID
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date November 1, 2020
Est. completion date June 1, 2024

Study information

Verified date December 2023
Source University of Chicago
Contact Matthew Bona
Phone 773-702-3560
Email dewitlab@yoda.bsd.uchicago.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this project, we will examine individual differences in the effects of a stimulant drug, methamphetamine (MA), on mesolimbic reward function using fMRI.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date June 1, 2024
Est. primary completion date October 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - BMI between 19 and 26 - Right Handed - Less than 4 alcohol or caffeinated beverages a day. Exclusion Criteria: - High blood pressure - 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.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Methamphetamine
Participants will be given 20 mg of Methamphetamine.
placebo oral tablet
Participants will be given a placebo capsule that will only contain lactose.

Locations

Country Name City State
United States University of Chicago Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
University of Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in SUbjective Effects as Assessed by Score on "Feel Drug", "Feel High", "Like Drug", and "Want More" Sub-scales of Drug Effects Questionnaire (DEQ). Participants will complete The Drug Effects Questionnaire during the initial baseline session to determine their subjective stimulant profile. The Dug Effects Questionnaire (DEQ) is a visual analog scale questionnaire that assesses the extent to which subjects experience four subjective states: "Feel Drug", "Feel High", "Like Drug", and "Want More". All sub-scales are scored on a visual analogue scale (Scroll bar on computer screen) ranging from 0-100. 100 represents the highest score for that subjective state, and the higher the score, the worse the outcome. Time Frame: Day 1(baseline), 3
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