🏛️ Verified NIH Record • Updated 2026-02-27

Endoscopic Sleeve Gastroplasty (ESG) Prospective Trial for Obesity (EGO-Trial) (NCT07449520)

Endoscopic Sleeve Gastroplasty (ESG) Prospective Trial for Obesity

🟡 Not Yet Recruiting Interventional Protocol 📊 Observational Clinical Research Sponsor: IHU Strasbourg

🩺 Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Hôpital Privé de Provence — Aix-en-Provence

Age range: 18 Years to 75 Years

🧪 Interventions in This Study

  • Endoscopic sleeve gastroplasty (PROCEDURE)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (10 Sites)

  • Hôpital Privé de Provence — Aix-en-Provence,
  • Polyclinique de Franche-Comté — Besançon,
  • Clnique des Cèdres — Échirolles,
  • Hôpital HURIEZ — Lille,
  • Hospices Civils de Lyon - Hôpital Edourard HERRIOT — Lyon,
  • Clinique Clémentville — Montpellier,
  • Centre Mutualiste de l'Obésité — Saint-Etienne,
  • Polyclinique Sainte Thérèse — Sète,
  • Hôpitaux Universitaires de Strasbourg, Nouvel Hôpital Civil — Strasbourg,
  • Clinique les Eaux Claires — Baie-Mahault,

📞 Contact the Study Coordinator

Phone: 0033 390 413608

Email: armelle.takeda@ihu-strasbourg.eu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Obesity clinical trials

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗