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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
France
CHU de Nice - Hôpital de l'Archet
RECRUITING
Nice
Contact Information
Primary
ROUX Christian, PhD
roux.c@chu-nice.fr
+3349209220
Backup
Iannelli Antonio, PhD
chirurgiedigestive@priannelli.com
Time Frame
Start Date: 2024-03-06
Estimated Completion Date: 2027-03-06
Participants
Target number of participants: 40
Treatments
Other: whole blood in a GLP1
Oxytocyne assay in a GLP1 analogue or non-analogue patient population
Other: whole blood in non analague patient population
Oxytocyne assay in a GLP1 analogue or non-analogue patient population
Related Therapeutic Areas
Sponsors
Leads: Centre Hospitalier Universitaire de Nice

This content was sourced from clinicaltrials.gov