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Clinical Trials/NCT02902198
NCT02902198RecruitingNot Applicable

Taste Physiology in Obese Volunteers Before and After Bariatric Surgery

University Hospital, Basel, Switzerland1 site in 1 country16 target enrollmentStarted: December 1, 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
16
Locations
1
Primary Endpoint
Effect of tastants on cerebral blood flow measured by functional brain MRI

Study Overview

Brief Summary

The objective is to investigate neuro-anatomical correlates of gastrointestinal taste stimulation by means of functional MRI before and after bariatric surgery. Intragastric administration of glucose, monosodium glutamate, chloroquine and placebo is followed by functional brain MRI in obese humans before and 3 months after surgery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Triple (Participant, Care Provider, Investigator)

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • morbidly obese patients (BMI min 35kg/m2) scheduled for bariatric surgery
  • right handed

Exclusion Criteria

  • cardiovascular disease
  • neurologic/psychiatric disorders

Outcomes

Primary Outcomes

Effect of tastants on cerebral blood flow measured by functional brain MRI

Time Frame: changes from baseline to one hour after treatment

Secondary Outcomes

  • Effect of tastants plasma glucagon-like peptide (GLP-1) concentrations(changes from baseline to one hour after treatment)
  • Effect of tastants plasma ghrelin concentrations(changes from baseline to one hour after treatment)

Investigators

Sponsor
University Hospital, Basel, Switzerland
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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