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ObesityNCT07449520

Endoscopic Sleeve Gastroplasty (ESG) Prospective Trial for Obesity (EGO-Trial)

An observational study of Obesity, run by IHU Strasbourg at 10 sites in 2 countries.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

EGO-Trial is the first multicenter study in France which aims to evaluate the efficacy of Endoscopic Sleeve Gastroplasty (ESG) in patients with obesity. This project fills a critical national gap by providing real-world, multicentric data from diverse French healthcare settings, offering insight into the safety… Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Obesity
What is being tested?
Endoscopic sleeve gastroplasty
Type of treatment
Surgery or procedure
How many people
300 participants
Where
10 sitesin 2 countries
Study dates
Mar 2026to Mar 2030
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients with obesity scheduled for endoscopic gastroplasty

Who may be able to join

  • Patients aged 18 to 75 years.
  • Patients with a Body Mass Index (BMI) ≥ 30 kg/m².
  • Patients who have failed non-surgical weight loss interventions (diet, exercise, pharmacological therapy).
  • Patients not eligible for bariatric surgery or does not wish to undergo it.
  • Patients who can undergo general anesthesia.
  • Patients who are able to participate in all aspects of the study and agree to comply with all study requirements for the entire duration of the study.
  • Patients who are able to fully understand the study and are willing to give their consent to participate in the study.
  • Patients affiliated with the French social security system.

Who cannot join

  • Patients with contraindications to endoscopic gastroplasty
  • Patients with active peptic ulcer disease or significant gastroparesis
  • Patients with a history of bariatric, gastric, or esophageal surgery.
  • Patients who have started medication in the last 3 months that is known to cause weight gain.
  • Patients with a history of uncontrolled, poorly controlled, or suspected eating disorders or psychiatric illness.
  • Patients with unstable and precarious health, as determined and assessed by the investigator.
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  • Patients who are pregnant, breastfeeding, or of childbearing age and not using effective contraception.
  • Patients who are currently excluded (as determined by a previous or ongoing study).
  • Patients under judicial protection.
  • Patients under guardianship, conservatorship or subject to any form of protective supervision

Trial locations and contacts

10 sites in 2 countries. Contact the study team or a site near you to ask about taking part.

Clinical Research Team contact

rc-ihu@ihu-strasbourg.eu

10 sites in 2 countries

France9 sites
  • Hôpital Privé de Provence

    Aix-en-Provence

    Hugues SEBBAG, 0033 4 42 21 12 11, hsebbag.ppr@hotmail.fr

  • Polyclinique de Franche-Comté

    Besançon

    Henry-Alexis MERCOLI, 0033 3 81 41 81 41, docteur.mercoli@gmail.com

  • Clnique des Cèdres

    Échirolles

    Fabien STENARD, 0033 4 56 58 14 90, fabien.stenard@cliniquedescedres.com

  • Hôpital HURIEZ

    Lille

    Robert CAIAZZO, 0033 3 20 44 42 73, robert.caiazzo@univ-lille2.fr

  • Hospices Civils de Lyon - Hôpital Edourard HERRIOT

    Lyon

    Maud ROBERT, 0033 4 72 11 62 61, Maud.robert@chu-lyon.fr

  • Clinique Clémentville

    Montpellier

    Marta SILVESTRI, 0033 4 67 06 70 00, docteur.m.silvestri@gmail.com

  • Centre Mutualiste de l'Obésité

    Saint-Etienne

    Pierre BLANC, 0033 4 77 81 82 88, PBLANC@mutualite-loire.com

  • Polyclinique Sainte Thérèse

    Sète

    Thibaut COSTE, 0033 4 67 18 88 20, thibautcoste@gmail.com

  • Hôpitaux Universitaires de Strasbourg, Nouvel Hôpital Civil

    Strasbourg

    Silvana PERRETTA, 0033 3 69 55 05 31, perretta@unistra.fr

Other trials in France

Guadeloupe1 site
  • Clinique les Eaux Claires

    Baie-Mahault

    Venetia AVENDANO, 0033 5 90 25 95 65, zulemacu@yahoo.com

Other trials in Guadeloupe

About this study

Official title: Endoscopic Sleeve Gastroplasty (ESG) Prospective Trial for Obesity

EGO-Trial is the first multicenter study in France which aims to evaluate the efficacy of Endoscopic Sleeve Gastroplasty (ESG) in patients with obesity. This project fills a critical national gap by providing real-world, multicentric data from diverse French healthcare settings, offering insight into the safety, efficacy, and variability of ESG practices across institutions

The project is expected to generate robust, multicentric clinical evidence on the safety and efficacy of ESG in patients with obesity within the French healthcare context.

Read the detailed description

Obesity, particularly morbid obesity, is a major public health issue in France. According to the latest data from the ObÉpi-Roche 2020 survey, more than 17% of French adults are obese. Obesity is a well-established risk factor for many chronic diseases such as type 2 diabetes, cardiovascular disease, high blood pressure (HBP), musculoskeletal disorders, certain cancers, and non-alcoholic steatohepatitis (NASH). It is associated with a significant reduction in life expectancy and represents a direct cost estimated at more than €5 billion per year for the French healthcare system.

While bariatric surgery (particularly sleeve gastrectomy and gastric bypass) remains the gold standard treatment for severe obesity, it is invasive, costly, and only offered to a minority of patients (less than 10% of eligible patients). In addition, certain medical contraindications, refusal of surgery, and waiting times limit access to this treatment.

Endoscopic sleeve gastroplasty ("Endosleeve"). Endoscopic sleeve gastroplasty (ESG) is an innovative, non-surgical, natural procedure that reduces stomach volume without resection or anastomosis. It has shown promising results in terms of weight loss, metabolic improvement, and safety, while being reversible and reproducible. The MERIT randomized controlled trial in USA (JAMA, 2022) demonstrated an average weight loss of 13.6% of total body weight at 12 months (vs. 0.8% in the control group), as well as a significant improvement in comorbidities such as type 2 diabetes and hypertension.

Hypothesis and objective of the study The hypothesis of this study is that ESG, when performed under routine care conditions in the United States, leads to significant and sustainable weight loss, associated with an improvement in comorbidities, with a favorable safety profile. The main objective of this project is therefore to evaluate, on a national scale, the clinical efficacy, safety, and procedural variability of ESG through a multicenter real-world cohort.

To date, no large-scale French study has analyzed the results of ESG in real-world settings. This hinders its integration into national healthcare pathways, its reimbursement by the French national health insurance system, and its wider adoption by the medical community. The question raised-the rigorous evaluation of ESG in the French context-therefore remains unanswered.

This project aims to generate robust data representative of the national clinical reality in order to support the supervised development of ESG. Expected outcomes include the publication of scientific articles in peer-reviewed journals, the presentation of results at international conferences, contributions to health technology assessment work, and the establishment of a national registry of endoscopic gastroplasty. This work could represent a major advance in the therapeutic arsenal for obesity, supporting the integration of ESG as a recognized, validated, and reimbursed option in French healthcare pathways.

Conditions
Obesity
Being tested
Endoscopic sleeve gastroplasty
Keywords
Obesity, Endoscopic Sleeve Gastroplasty, Excess weight loss, Body Mass Index, Quality of Life
Medical subject headings
Obesity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Endoscopic sleeve gastroplastyProcedure or surgery

    Endoscopic sleeve gastroplasty is performed using a CE marked endoscopic suture device which allows for a reduction in stomach volume without resection or anastomosis

Study groups in NCT07449520
Study groupRoleWhat they receive
All adult patients with obesity scheduled for endoscopic gastroplasty (ESG)Not described
Receives: Procedure: Endoscopic sleeve gastroplasty

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Total Body Weight Loss

    Assessment of weight loss in terms of total body weight loss (TBWL, %) 24 months after surgery

    Measured: At the inclusion and 24 months after procedure

Secondary outcomes (6)
  1. Excess weight loss

    Assessment of weight loss in terms of excess weight loss (EWL, %) at 24 months post-procedure

    Measured: At the inclusion and 24 months after procedure

  2. Body Mass Index (BMI)

    Assessment of weight loss in terms of change in Body Mass Index (BMI) at 24 months post-procedure

    Measured: From ESG procedure to the end of participation at 24 months post-procedure

  3. Adverse events

    Rate of minor and major adverse events (e.g., perforation, delayed gastric emptying, reflux symptoms) throughout follow-up for up to 24 months post-procedure

    Measured: From ESG procedure to the end of participation at 24 months post-procedure

  4. Comorbidities improvement

    Assessment of improvement in comorbidities (type 2 diabetes, hypertension, dyslipidemia, sleep apnea) and obesity-related complications over 24 months using the SF-BARI (Swiss-Finnish BARIatric metabolic outcome score) questionnaire: a score developed to evaluate treatment outcomes in obesity management

    Measured: From ESG procedure to the end of participation at 24 months post-procedure

  5. Quality of life improvement

    Assessment of quality of life over 24 months using the GIQLI (Gastrointestinal Quality of Life Index) questionnaire: digestive quality of life score comprising 36 items relating to symptoms, physical status, emotions, social problems, and the effect of medical treatments

    Measured: From ESG procedure to the end of participation at 24 months post-procedure

  6. Additional treatments

    Compilation of additional treatments or revisions required after the procedure

    Measured: From ESG procedure to the end of participation at 24 months post-procedure

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Mar 2026
  2. Study startMar 2026 (estimated)
  3. Primary completionMar 2030 (estimated)
  4. Study completionMar 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07449520
Sponsor's protocol ID
25-004
Status last verified
Feb 2026
First submitted
27 Feb 2026
Last updated
4 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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