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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02589613
Other study ID # fMRI Obese
Secondary ID
Status Completed
Phase N/A
First received October 20, 2015
Last updated October 26, 2015
Start date October 2013
Est. completion date June 2014

Study information

Verified date October 2015
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Interventional

Clinical Trial Summary

The objective is to investigate neuro-anatomical correlates of the regulation of energy intake by means of functional MRI. Administration of glucose as well as fructose is followed by functional brain MRI, and findings are correlated with serum glucagon-like peptide 1 (GLP-1) levels as an endogenous satiety signal in obese humans.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date June 2014
Est. primary completion date June 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- right-handed healthy males, no drugs, non-smoking

Exclusion Criteria:

- drug abuse, smoker, left-handed, claustrophobia

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
tap water
300ml tap water via nasogastric tube
Glucose
300ml tap water with 75g Glucose via nasogastric tube
Fructose
300ml tap water with 25g Fructose via nasogastric tube

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Outcome

Type Measure Description Time frame Safety issue
Primary Functional magnetic resonance imaging (fMRI) in healthy, obese volunteers while they performed a working memory task: changes in cerebral blood flow changes from baseline to one hour after treatment No
Secondary Changes in plasma insulin changes from baseline to one hour after treatment No
Secondary Changes in plasma glucose changes from baseline to one hour after treatment No
Secondary Changes in plasma GLP-1 changes from baseline to one hour after treatment No
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