Impact of a Pro-diversity Gut Microbiota Diet After a Bariatric Surgery on Gut Microbiota, Eating Behaviour and Sensory Function

Last updated: April 2, 2026
Sponsor: Hospices Civils de Lyon
Overall Status: Active - Recruiting

Phase

N/A

Condition

Diabetes Prevention

Obesity

Weight Loss

Treatment

Nutritional counseling

Clinical Study ID

NCT07268508
69HCL24_0033
  • Ages 25-65
  • All Genders

Study Summary

Bariatric surgery is the most effective treatment for long-term weight loss and reducing obesity-related health risks. It alters the gastrointestinal tract as well as metabolic and hormonal functions, influencing eating behaviour. However, weight loss outcomes and long-term maintenance vary between patients, likely due to changes in the gut microbiota. Dietary recommendations aimed at improving microbiota diversity could help support sustained weight loss after surgery.

The BariaGut Taste study aims to compare two dietary approaches following bariatric surgery: nutritional counselling promoting gut microbiota diversity versus standard nutritional counselling. One year after surgery, the study will evaluate differences in microbiota diversity, changes in food preferences and eating behaviours, sensory profiles (taste, smell), levels of digestive and gut hormones fasting, before and after eating, cardiometabolic parameters, mental health, physical activity, and more, to better understand Bariatric surgery is the most effective treatment for long-term weight loss and reducing obesity-related health risks. It alters the gastrointestinal tract as well as metabolic and hormonal functions, influencing eating behaviour. However, weight loss outcomes and long-term maintenance vary between patients, likely due to changes in the gut microbiota. Dietary recommendations aimed at improving microbiota diversity could help support sustained weight loss after surgery.

The BariaGut Taste study aims to compare two dietary approaches following bariatric surgery: nutritional counselling promoting gut microbiota diversity versus standard nutritional counselling. One year after surgery, the study will evaluate differences in microbiota diversity, changes in food preferences and eating behaviours, sensory profiles (taste, smell), levels of digestive and gut hormones fasting, before and after eating, cardiometabolic parameters, mental health, physical activity, and more, to better understand the mechanisms that may explain variations in response to bariatric surgery.

The BariaGut Taste study is a prospective, randomized, controlled trial with two parallel groups, involving non-diabetic patients aged 25 to 65 y undergoing either sleeve gastrectomy or Roux-en-Y gastric bypass. The trial will be conducted at the digestive surgery department of Edouard Herriot Hospital, the endocrinology-diabetes-nutrition department of Lyon Sud Hospital Center, and the Human Nutrition Research Center Rhône-Alpes. 60 participants are expected to be recruited, with 30 in each arm.

Participants will be enrolled before surgery during a routine care visit with the surgeon. They will then undergo a metabolic assessment visit conducted exclusively for research purposes. This visit will allow to collect baseline data on primary outcomes via blood, expired air, and stool samples, anthropometric measurements, indirect calorimetry, a battery of questionnaires (TFEQ-21, DEBQ, PHQ-9, SF36, GSES, PANAS, ESUL, BES, DERS, GAD-7, IPAQ, BAQ, GSRS, sensory alterations, Bristol and Likert scales, and FNS), computerized food preference tests (LFPQ), and a standardized, video-recorded ad libitum buffet.

Participants will be followed up at 3, 6, and 12 months after surgery through visits combining clinical care and research assessments. The dietary interventions specific to each group will be provided since the 3-month visit. The assessments conducted before surgery will be repeated at 6 and 12 months, also integrating clinical care objectives.

Additional blood, stool, and adipose tissue samples collected during surgery will be stored to create a biobank.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Between 25 and 65 years old

  • Undergoing either sleeve gastrectomy or Roux-en-Y gastric bypass

  • With grade 3 obesity (BMI≥40 kg/m²) or with BMI≥35 kg/m² and at least onecomorbidity likely to be improved after surgery, with the exception of type 2diabetes

  • Signed consent form

  • Living less than an hour and 30 minutes from the hospital

  • Presence of effective and stable contraception for women of childbearing potential

Exclusion

Exclusion Criteria:

  • Type 2 diabetes

  • Presence of a contraindication to bariatric surgery

  • Presence of gastrointestinal pathologies with an inflammatory component, knowngastroparesis, total gastrectomy, colectomy, exocrine pancreatic insufficiency,known endocrine pathologies inducing hyperglycaemia (uncontrolled dysthyroidism,acromegaly, hypercorticism, etc.), severe chronic renal insufficiency (< 30mL/min),or hepatocellular insufficiency

  • Claustrophobic

  • Pregnant or breastfeeding women

  • Taking an obesity treatment 3 months before surgery

  • Taking a corticoids, immunosuppression, anabolizing, or growing hormones, antibodytreatments less than 3 months before inclusion

  • Daily taking of laxatives or drugs that can strongly interfere with the compositionof the intestinal microbiota. If taken sporadically, the patient can be included ata distance (3 weeks) from the laxatives taken.

  • Specific diets (vegetarian, vegan or without gluten)

  • No French speaker

  • Already included in other study

  • Donated blood in the last two months

  • Without freezer access

  • With allergy or intolerance to food propose in ad libitum buffet

Study Design

Total Participants: 60
Treatment Group(s): 1
Primary Treatment: Nutritional counseling
Phase:
Study Start date:
November 05, 2025
Estimated Completion Date:
April 05, 2029

Connect with a study center

  • Hospital Edouard Herriot, digestive surgery department

    Lyon, 69310
    France

    Active - Recruiting

  • Hospital Edouard Herriot, digestive surgery department

    Lyon 2996944, 69310
    France

    Site Not Available

  • Centre de recherche en nutrition humaine de Rhône-Alpes

    Pierre-Bénite, 69310
    France

    Site Not Available

  • Hôpital Lyon sud, Endocrinology Diabetes Nutrition department

    Pierre-Bénite, 69310
    France

    Site Not Available

  • Centre de recherche en nutrition humaine de Rhône-Alpes

    Pierre-Bénite 2987314, 69310
    France

    Site Not Available

  • Hôpital Lyon sud, Endocrinology Diabetes Nutrition department

    Pierre-Bénite 2987314, 69310
    France

    Site Not Available

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.