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Effects of Roux-en-Y Gastric Bypass on Gastro-intestinal Hormone Secretion and Brain Responses Food Pictures

U

University of Lausanne (UNIL)

Status

Completed

Conditions

Obesity

Treatments

Other: standard test meal

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This is a cross-sectional study enrolling

  • 11 weight-stable, formerly obese female patients 1-5 years after Roux-en-Y gastric Bypass (RYGB)
  • 11 age- and weight-matched female subjects
  • 10 normal weight (Body Mass Index 19-25 kg/m2) subjects The following measurements will be performed in each participants in basal conditions (after an overnight fast) and after ingestion of a standard meal
  • electroencephalographic recordings of visually evoked potential after presentation of food- or non-food pictures
  • plasma concentration of metabolites (glucose, fatty acids), glucoregulatory hormones (insulin, glucagon), gastro-intestinal hormones (Gastric Inhibitory Polypeptide (GIP), Glucagon-like Peptide-1 (GLP1), ghrelin,Cholecystokinin (CCK), and bile acids Aims of this observational study are
  • to evaluate the effects of RYGB on brain perception of food related visual stimulation
  • to search for relationships between RYGB effects on brain responses and gastro-intestinal hormone secretion

Enrollment

31 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • good apparent health
  • gender: female
  • age 18-50
  • non-smoker

Exclusion criteria

  • diabetes or antidiabetic medication
  • consumption of more than 50g alcohol per week
  • vegetarian or any special diet

Trial design

31 participants in 3 patient groups

post Roux-en-Y-gastric bypass
Description:
Formerly obese females 1-5 years after gastric bypass
Treatment:
Other: standard test meal
matched controls
Description:
non-operated females age-and weight-matched to post Roux-en-Y-gastric bypass subjects
Treatment:
Other: standard test meal
healthy young controls
Description:
non overweight (BMI between 19 and 25 kg/m2) healthy females
Treatment:
Other: standard test meal

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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