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NCT03821636Recruiting

Impact of Long Alimentary Limb or Long Biliary Limb Roux-en-Y Gastric Bypass on Type 2 Diabetes Remission in Severely Obese Patients.

Impact of Long Alimentary Limb or Long Biliary Limb Roux-en-Y Gastric Bypass on Type 2 Diabetes Remission in Severely Obese Patients. A Prospective, Multicentric, Randomized, Controlled Trial.

Source: ClinicalTrials.gov · Last updated 23 Dec 2025

Brief summary (registry, in English)

In patients with type 2 diabetes, Roux-en-Y gastric bypass (RYGB), which excludes a portion of the stomach and the proximal intestine from the alimentary circuit, improves glucose metabolism more rapidly and more extensively than is expected from weight loss. The mechanisms of this unique effect of gastrointestinal exclusion appear to be complex and have not yet been clarified. A recent study unveil that intestinal uptake of ingested glucose is diminished by RYGB and restricted to the common limb, where food meets bile and other digestive fluids, resulting in an overall decrease of post prandial blood glucose excursion. the hypothesize that reducing the length of the common limb, which is rarely measured and highly variable in clinical practice, may significantly affect the metabolic outcome of gastrointestinal surgical procedures. The aim of the present study is to compare the impact of two variants of Roux-en-Y gastric bypass with a short common limb, the long alimentary limb or the long biliary limb Roux-en-Y gastric bypass, on type 2 diabetes remission in severely obese patients.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
396 (estimated)
First submitted
26 Nov 2018
Start date
16 Jun 2019
Primary completion date
Jun 2026
Lead sponsor
University Hospital, Lille
NCT number
NCT03821636

What you commit to

  • Study type: Interventional
  • Planned participants: 396
  • From 16 Jun 2019 to the primary completion date, Jun 2026
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • patient who have already undergone obesity surgery
  • The absence of identified prior medical management of obesity

Other illness

  • Severe cognitive or mental disorders
  • Severe and non-stabilised eating disorders
  • Diseases that are life-threatening in the short and medium term;

Other

  • The likely inability of the patient to participate in lifelong medical follow-up
  • Alcohol or psychoactive substances dependence
  • Contraindications to general anaesthesia.

Who the study is looking for

  • BMI ≥ 35 kg/m2
  • All patient with type 2 diabetes
  • Patients who were candidates for obesity surgery in accordance with French recommendation

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chu Amiens Picardie
Coordinator of this site? Confirm its status
AmiensFranceRecruiting
Ch Boulogne-Sur-Me
Coordinator of this site? Confirm its status
Boulogne-sur-MerFranceRecruiting
Hop Claude Huriez Chu Lille
Coordinator of this site? Confirm its status
LilleFranceRecruiting
CH de Valenciennes
Coordinator of this site? Confirm its status
ValenciennesFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.