Control of Cognition (Naltrexone, Methylphenidate, and ADHD Study (NMAS))
NCT01993108 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 23
Last updated 2018-06-18
Summary
The goal of this research is to understand the functioning of 'regulatory circuits' in the brain. We are also interested in how the medications methylphenidate and naltrexone affect these regulatory circuits. This research study will use a scanning technique known as functional magnetic resonance imaging (fMRI) which takes a special kind of picture of the brain that enables us to "see the brain at work". Adult participants will be given a one-time dose of either methylphenidate, naltrexone,or placebo before each fMRI scan session.
The main purpose for this research is to better understand the functioning of regulatory circuits in healthy individuals and individuals with psychiatric disorders. This research may one day help us develop better treatments for these disorders.
Conditions
- Healthy
- Attention Deficit Hyperactivity Disorder
Interventions
- DRUG
-
Methylphenidate
One dose 40mgs of methylphenidate one hour before fMRI scanning.
- DRUG
-
Naltrexone
One dose 40mgs of naltrexone one hour before fMRI scanning.
- DRUG
-
One dose of placebo one hour before fMRI scanning.
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Chandra Sekhar Sripada, MD, PhD · University of Michigan
Study Design
- Allocation
- RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 35 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2013-10-31
- Primary Completion
- 2015-12-31
- Completion
- 2017-02-28
- FDA Drug
- Yes
Countries
- United States
Study Locations
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