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Identification of Factors Predictive of the Efficacy of Endoscopic Endoscopic Sleeve Gastroplasty & Study the Evolution of Clinical, Biological and Intestinal Intestinal Microbiota After Surgery

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

Endoscopic sleeve gastroplasty and bypass are currently available for weight loss in obese patients who have failed nutritional management. Despite very low risks, these techniques remain invasive. What's more, the French National Authority for Health recommends this procedure for patients with a BMI above 35 kg/m² with associated co-morbidities, or above 40 kg/m². This excludes grade I obese patients (30 \< BMI \< 35) who have no effective means of losing weight. The hospital's hepato-gastroenterology and nutrition department has therefore implemented endoscopic sleeve gastroplasty to address this problem. As with other surgical techniques, there is heterogeneity heterogeneity in weight loss. The investigators therefore aim to identify factors predictive of the efficacy of this procedure in order to improve patient management of patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient of legal age (Age ≥ 18 years)

• Patient capable of understanding the study and signing a consent.

• BMI between 30 and 35 kg/m² with the presence of at least one one obesity-related complication (diabetes, dyslipidemia, sleep apnea syndrome, non-alcoholic steatohepatitis, joint pain joint pain).

• Patients with a BMI greater than 35 kg/m² who have been bariatric surgery has been refused.

• Patient who has failed to lose weight and improve with conventional techniques.

• Patient affiliated to a social security scheme

Locations
Other Locations
France
Hôpital Antoine Béclère
RECRUITING
Paris
Contact Information
Primary
Cosmin VOICAN, MD, PhD
cosmin.voican@aphp.fr
1 45 37 47 75
Backup
Gabriel PERLEMUTER, MD, PhD
gabriel.perlemuter@aphp.fr
1 45 37 47 75
Time Frame
Start Date: 2025-09-09
Estimated Completion Date: 2031-02-02
Participants
Target number of participants: 205
Related Therapeutic Areas
Sponsors
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov