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Clinical Trials in France / NCT06278285
Recruiting Not applicable

Effect of Agonist GLP1 on Adipose Tissue in Patients Undergoing Bariatric Surgery

NCT06278285 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-03-06
Last updated
2026-03-27

Condition(s) studied

Obesity

Investigational drug(s) / intervention(s)

Blood GLP1Blood No treated GLP1

Blood GLP1: On the day of surgery, the surgeon will remove visceral adipose tissue (1 cm3) from the operative waste. The adipose tissue is separated into 2 samples, one frozen in nitrogen, the other embedded in formalin. The samples are then sent to the Institut de Biologie de Valrose (iBV) to assess any differences between the two groups of patients (patients treated with anti-GLP-1 analogues

Blood No treated GLP1: On the day of surgery, the surgeon will remove visceral adipose tissue (1 cm3) from the operative waste. The adipose tissue is separated into 2 samples, one frozen in nitrogen, the other embedded in formalin. The samples are then sent to the Institut de Biologie de Valrose (iBV) to assess any differences between the two groups of patients (patients treated with patients not treated with anti-GLP-1 analogues) and the presence of fibrosis.

Study summary

Normalizing weight gain and preventing the redistribution of body fat is a major health issue, and could help prevent the onset of various symptoms of metabolic syndrome. Above all, it is important to understand the mechanisms by which these different treatments affect adipose tissue. To this end, the investigators will first study the impact of GLP-1 analogues on adipose tissue. The main objective is to show that subjects treated with a GLP-1 agonist have a significant change in their oxytocin levels compared with subjects not treated with a GLP-1 agonist.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient over 18 years of age. * Patient able to read and understand the information/consent leaflet. * Patient with BMI \> 35 with at least one comorbidity. Or BMI \> 40 * Indication for digestive surgery validated in a multidisciplinary consultation meeting and prior agreement accepted by the CPAM. * Membership of a social security scheme * Patient's signed informed consent * For subjects in the GLP-1 analogue group: GLP-1 analogue taken for at least 3 months. * For non-GLP-1 analogue group: never taken GLP-1 analogues. Exclusion Criteria: * Pregnant or breast-feeding women. * Vulnerable patients (under guardianship) * Patients deprived of liberty

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHU de Nice - Hôpital de l'Archet Nice Alpes-maritimes Recruiting

More Centre Hospitalier Universitaire de Nice trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06278285 on ClinicalTrials.gov ↗ ← All trials in France