Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06057597

Omega Gastric Bypass (150cm) Compared to the Roux-en-Y Gastric Bypass (YOMEGA-2 Multicentric Trial)

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2026-02-27

368

Participants Needed

1

Research Sites

263 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Obesity with its consequences such as type 2 diabetes, high blood pressure, dyslipidemia, fatty liver disease, sleep apnea and cancers, remains a major healthcare problem worldwide. Bariatric surgery, combined with nutritional education and close monitoring, has been shown to be the most effective treatment for patients with morbid obesity resulting in significant and lasting weight loss and improvements in co-morbidities . With nearly 50000 procedures per year France ranks third in the world in terms of care for patients suffering from morbid (BMI ≥ 40 kg/m²) and severe (BMI 35-40 kg/m²) obesity. In parallel with the significant increase in the number of patients operated on for obesity in the world, over the past two decades, significant development has been observed in the field of bariatric surgery with a decrease or even disappearance of some procedures and the appearance of others. Performed for more than 40 years, the Roux-en-Y Gastric Bypass (RYGB) is a restrictive and malabsorptive procedure and currently is considered as gold standard procedure for the treatment of morbid obesity and its comorbidities. However, despite the good effectiveness (with an average Excess Weight Loss % (EWL%) of approximatively 70% at 2 years), RYGB is technically demanding procedure with learning curve requiring more than 100 cases and an overall complication rate ranging from 10% to 20% Introduced in 2001, one anastomosis gastric bypass (OAGB) is a modified gastric bypass that consists of a single gastrojejunal anastomosis between a long gastric pouch and a jejunal (biliopancreatic) omega loop. In Sept. 2019, taking into account the results from YOMEGA trial, the French High Authority for Health (Haute Autorité de Santé (HAS)) recommended to ban OAGB with 200 cm or longer BPL and urged to assess the efficacy and safety of OAGB with 150 cm BPL in a randomized controlled trial. Indeed, YOMEGA-2 trial is logical continuity of the YOMEGA trial. The aim of this study is to assess weight loss efficiency and the nutritional safety of the OAGB-150 in comparison to a standard (RYGB). The hypothesis of this study is that the OAGB with a 150 cm BPL could have the same efficacy on weight loss and nutritional complication rate in comparison to the RYGB at 2 years.

CONDITIONS

Official Title

Omega Gastric Bypass (150cm) Compared to the Roux-en-Y Gastric Bypass (YOMEGA-2 Multicentric Trial)

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient aged from 18 to 65 years old
  • Type III obesity (BMI 240 kg/m2), or Type II obesity (BMI 35-40 kg/m2) with at least one related health problem (high blood pressure, type 2 diabetes, sleep apnea, dyslipidemia, or arthrosis)
  • Upper gastrointestinal endoscopy with biopsies to check for Helicobacter pylori within 12 months before surgery
  • Multidisciplinary evaluation lasting at least 6 months with a positive recommendation for gastric bypass
  • Understanding and acceptance of the need for long-term follow-up
  • Agreement to participate in the study with signed informed consent
  • Affiliated with a social security scheme
  • Effective contraception for women of childbearing age
Not Eligible

You will not qualify if you...

  • Previous bariatric surgery
  • Chronic inflammatory bowel disease
  • Chronic diarrhea
  • Severe, life-threatening progressive illness
  • Gastric mucosa changes such as dysplasia, chronic atrophic gastritis, or history of gastric cancer
  • Unhealed gastro-duodenal ulcer
  • Helicobacter pylori infection resistant to treatment
  • Esophagitis
  • Pregnancy or desire to become pregnant during the study
  • Mental instability, under supervision or guardianship
  • Inability to understand French or give informed consent
  • Participation in another interventional trial
  • Unable to consent due to legal protection or judicial guardianship
  • Type 1 diabetes

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Hôpital Bichat Claude-Bernard

Paris, France

Actively Recruiting

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Research Team

T

Tigran POGHOSYAN, MD-PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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