National Registry of Obesity Treatment by Endosleeve

ConditionObesity
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorSociété Française d'Endoscopie Digestive

About this trial

Obesity and overweight have emerged as public health problems of a pandemic nature, significantly reducing the life expectancy of those affected. Obesity has a considerable medico-economic impact, linked to the treatments it requires and its comorbidities. Currently, the prevention of obesity in our Western societies is not effective enough, as the prevalence and incidence of obesity and overweight continue to rise worldwide. In France, the therapeutic management of this condition is governed by the HAS and is summarized as a surgical approach for type 2 obesity with comorbidity or type 3 obesity, with three authorized methods that have shown sufficient evidence: gastric banding, sleeve gastrectomy (or longitudinal sleeve gastrectomy), and Roux-en-Y gastric bypass.

With the advent of organ-preserving interventional endoscopy, the systematic use of these surgical methods, although effective for total weight loss and excess weight loss, raises questions. Indeed, these new therapeutic endoscopic approaches, which are less invasive, less costly, and respectful of anatomy, currently show convincing cohort results in the short term (12 to 24 months) and require confirmation of their effectiveness and safety in the long term (5 years) so that they can become first-line therapeutic methods in the near future. At the request of the HAS in its self-referral of 2020 and then in 2022, this prospective registry aims to confirm the effectiveness and safety of the endosleeve (or endoscopic sleeve) in the long-term therapeutic management of obesity within the framework of everyday practice in national reference centers for obesity treatment.

Eligibility criteria

Qualifiers

Age over 18 years;

Patient with a body mass index (BMI) ≥ 30 kg/m²;

Signed informed consent

Disqualifiers

Contraindication to performing an upper endoscopy or using an endoscopic plication system according to the instructions for use (IFU);

Presence of an ulcer in the gastric body or fundus;

Achalasia, severe esophagitis (Los Angeles grade C or D);

ENT or esophageal malformation;

Trial design

Treatments tested in this trial

  • Therapeutic endoscopy endosleeve using a gastric suturing device (OverStitch™/Endomina™)

Treatment groups

354 Participants
are divided into 1 treatment group

Locations

This trial has no locations