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.
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
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
Guadeloupe1 site
Clinique les Eaux Claires
Baie-Mahault
Venetia AVENDANO, 0033 5 90 25 95 65, zulemacu@yahoo.com
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 group | Role | What 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.
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)
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
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
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
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
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
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.
- First posted4 Mar 2026
- Study startMar 2026 (estimated)
- Primary completionMar 2030 (estimated)
- Study completionMar 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ObesityStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- IHU Strasbourg
- Sponsor type
- University, hospital or other
- Collaborators
- SOFF.COMM, Boston Scientific International S.A.
- Responsible party
- Sponsor
- Investigators
- Silvana PERRETTA, MD-PhD, Principal investigator, Hôpitaux Universitaires de Strasbourg
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