- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01906411
Dopaminergic Function and Food Reward
May 28, 2015 updated by: Sabine Frank, University Hospital Tuebingen
The broad aim of the study is to obtain a better understanding of alterations in mesolimbic reward pathways in adiposity based on the hypothesis of a hypofunctioning reward system in obesity.
This will be achieved by integrating a functional neuroimaging (fMRI) with behavioral reward tasks and the modulation of the dopamine level by dopamine depletion.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
36
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Tuebingen, Germany, 72076
- University Clinic of Tuebingen, MEG Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 45 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
community sample
Description
Inclusion Criteria:
- female
- healthy
Exclusion Criteria:
- fMRI contraindications
- claustrophobia
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
subjecst with different BMI
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Differential brain functions in the dopaminergic reward system
Time Frame: 4 hours after intake of the dopamine depletion or balanced aminoacid drink
|
differential brain fuctions will be measured by blood oxygen level dependent effect.
|
4 hours after intake of the dopamine depletion or balanced aminoacid drink
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
amino acid level changes due to dopamine depletion
Time Frame: 4 hours after intake of the dopamine depletion or balanced aminoacid drink
|
4 hours after intake of the dopamine depletion or balanced aminoacid drink
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Primary Completion (Actual)
March 1, 2014
Study Registration Dates
First Submitted
July 8, 2013
First Submitted That Met QC Criteria
July 19, 2013
First Posted (Estimate)
July 24, 2013
Study Record Updates
Last Update Posted (Estimate)
May 29, 2015
Last Update Submitted That Met QC Criteria
May 28, 2015
Last Verified
May 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DAD
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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