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NCT Number: NCT04915014

Sleeve Gastrectomy With Transit Bipartition(SG+TB) Versus Roux-en-Y Gastric Bypass (RYGB) for Type 3 Obesity

Obesity is a major public health problem worldwide. Bariatric surgery has proved to be the most effective treatment of morbid obesity in terms of weight reduction and remission of co-morbid conditions during long-term follow-up. Sleeve Gastrectomy (SG) has become the most performed intervention either worldwide or in France, where SG represents more than 60% of bariatric interventions and 114,817 patients operated between 2013 and 2016.

Maximum Excess weight loss (%EWL) after SG is obtained at one-year post surgery. Then it has been largely reported in the literature that patients could present mild, moderate or important (notably in the super obese patients) weight regain associated with comorbidity relapse motivating redo surgery. Like in revisional surgery, operating super-obese patient (BMI ≥50 kg/m2) is a challenge. It has been shown that achieving significant weight loss was more difficult in patients with a BMI ≥ 50 compared to lower BMIs.

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Key information

Conditions

Severe Obesity Body Weight Diabetes Mellitus Diabetes Mellitus, Type 2 Endocrine System Diseases Glucose Metabolism Disorders Hyperinsulinism Insulin Resistance Malnutrition Metabolic Diseases Metabolic Syndrome Nutrition Disorders Nutritional and Metabolic Diseases Obesity Obesity, Morbid Overnutrition Overweight Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hop Claude Huriez Chu Lille, Lille, France

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About this study

In these 2 populations of patients, more malabsorptive procedures like long limb One Anastomosis Gastric Bypass or Bilio-Pancreatic Diversion with Duodenal Switch could be more efficient but induce technical difficulties (high complication rate) and can be responsible for malnutrition (vitamin deficiencies, hypoalbuminemia…). That's why, in case of revisional surgery or for high BMI patients,laparoscopic Roux-en-Y gastric bypass (RYGBP) is still considered as the gold standard and is the most performed intervention. To obtain better weight loss safely,Santoro et al. promoted the sleeve gastrectomy with transit bipartition (SG+TB), a new intervention coupling a SG without interrupting pathway through the duodenum and preserving the pylorus and a long biliary limb RYGBP.

Hypothesis: Because there is no duodenal and jejunal exclusion, malnutrition is expected to be less frequent after SG+TB compared to BPD/DS. Its anastomosis on the antrum makes SG+TB easier to perform in super-obese patient than standard RYGB but more efficient in term of weight loss. Compared to BPD/DS or SADI which involves dissection of the duodenum and the confection of a duodenojejunostomy, SG+TB is also expected to be easier then safer.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient who has benefited from a pluridisciplinary evaluation, with a favorable opinion for SG+TB or RYGB as a first intention procedure with BMI ≥40 kg/m2 or BMI ≥ 35 kg/m2 associated with one co-morbidity which will be improved by surgery (according to HAS 2009 recommendation3) OR as a second intention procedure (revisional surgery) after failure of Sleeve gastrectomy (defined as insufficient weight loss at 18 months after surgery (EWL% <50), or as weight regain (+ 20%)).
  • Patient who had benefited from an Upper GI Endoscopy with biopsies to look for Helicobacter Pylori (HP) and a HP eradication.
  • Patient who understands and accepts the need for a long-term follow-up
  • Patient who agrees to be included in the study and who signs the informed consent form
  • Patient affiliated to a healthcare insurance plan

Exclusion criteria

  • History of previous bariatric surgery, other than a Sleeve Gastrectomy
  • Patient with current BMI > 60 kg/m2
  • Presence of a severe and evolutive life threatening pathology, unrelated to obesity
  • History of Chronic inflammatory bowel disease
  • Type 1 Diabetes
  • Pregnancy or desire to be pregnant during the study
  • Nursing woman
  • Presence of Pylori Helicobacter resistant to medical treatment
  • Presence of a non-healed gastro-duodenal ulcer or diagnosed less than 2 months previously
  • Severe esophagitis (grade C of Los Angeles classification)
  • Hiatal hernia
  • Patients with unstable psychiatric disorder, under supervision or guardianship
  • Patient who does not understand French/ is unable to give consent
  • Patient not affiliated to a French or European healthcare insurance
  • Patient who has already been included in a trial which has a conflict of interests with the present study
  • Patient incarcerated

Treatment and study plan

sleeve gastrectomy with transit bipartition (SG +TB)

Procedure

In case of a first intention procedure, a typical sleeve gastrectomy is performed, calibrated on a 36 French bougie, stapling starting 4 to 6 cm from the pylorus. Antecolic gastroileal anastomosis is performed 250 cm from the ileocecal transition, on the antrum using a linear stapler (45-mm gold cartridge) or hand-sewn (at least 3 cm wide on the stomach). Laterolateral enteroanastomosis is performed 120 cm from the ileocecal junction. Thus, alimentary limb is 130cm and common limb 120cm.

Roux-en-Y Gastric Bypass (RYGB)

Procedure

A small gastric pouch (30 cc) is performed. Antecolic gastroileal anastomosis is performed 200 cm from the Treitz junction, using a linear stapler (45-mm gold cartridge) or hand-sewn (at least 3 cm wide on the stomach). Laterolateral enteroanastomosis is performed 50 cm from the Treitz junction. Thus, alimentary limb is 150cm and biliary limb 50cm.

Primary outcomes

  1. The Excess Weight Loss percentage (EWL%)

    Time frame: at 2 years after surgery

    The Excess Weight Loss percentage (EWL%) calculated with the following formula: ((weight at 2 years visit - initial weight (kg)) / (initial weight - ideal weight)) X 100 Ideal weight defined as the weight corresponding to a BMI = 25 kg/m2. Initial weight defined as preoperative weight at V1. All weights are expressed in kg

Secondary outcomes

  1. Change nutritional status assessment

    Time frame: from baseline (before surgery) to 24 months after surgery

    Nutritional profil : Hemoglobin (g/l), albumin (g/l), prealbumin (g/l)

  2. Change in liver status assessment

    Time frame: from baseline (before surgery) to 24 months after surgery

    Liver parameters ( ALT AST GGT Alkaline phosphatases, Total bilirubin, prothrombin time, urea, creatininemia concentration)

  3. Change in vitamins status assessment

    Time frame: from baseline (before surgery) to 24 months after surgery

    vitamins profil (vitamin A B1, B6 B9, B12, C , D and E concentration)

  4. Change in mineral status assessment

    Time frame: from baseline (before surgery) to 24 months after surgery

    Mineral profil ( ferritin, potassium, calcium,iron, transferrin, magnesium, selenium, zinc phophore concentration)

  5. 24-hour steatorrhea quantified at 6 months

    Time frame: At 6 months

    24-hour steatorrhea is assessed to evaluate denutrition, expressed in g of lipid/24hr

  6. Evolution of muscle mass assessed by bioelectrical impedance analysis

    Time frame: from baseline to 24 months after surgery

    muscle mass is assessed to evaluate denutrition.

  7. Evolution of muscle mass assessed by grip strength test.

    Time frame: from baseline to 24 months after surgery

    muscle mass is assessed to evaluate denutrition.

  8. Complications rate within 2 years according to Dindo-Clavien classification

    Time frame: within 2 years

    complications rate is assessed to evaluate safety of the procedure

  9. Length of hospital stay defined as the number of days of hospitalization

    Time frame: up to 2 week

    length of hospital stay for the surgical procedure

  10. Evolution from baseline to 24 months after surgery of HbA1c level, HDL, LDL and triglycerides

    Time frame: from baseline to 24 months after surgery

    Evolution from baseline to 24 months after surgery of HbA1c level (expressed in %), fasting glycemia (expressed in mmol/l or g/l), HDL (expressed in mmol/l or g/l), LDL (expressed in mmol/l or g/l) and triglycerides (expressed in mmol/l)

  11. Evolution from baseline to 24 months of insulinoresistance defined by HOMA-IR calculated with fasting blood glucose and fasting insulinemia12

    Time frame: from baseline to 24 months

    assessment of insulinoresistance

  12. Change of the GIQLI score

    Time frame: from baseline to 24 months after surgery

    This questionnaire consists of 36 items exploring 5 dimensions or subscales: symptoms, physical condition, emotions, social integration and the effect of any medical treatment. For each item, 5 responses will be proposed to patients and for each answer, a score is assigned, ranging from 0 to 4 (highest score = 144). A high score defines a more favorable health state

  13. Change of the SF36 scores

    Time frame: from baseline to 24 months after surgery

    This questionnaire taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. It also includes a single item that provides an indication of perceived change in health.

  14. Change in Sigstad questionnaire score (dumping syndrome).

    Time frame: from baseline to 24 months after surgery

    The Sigstad questionnaire allows the identification and diagnosis of postoperative hypoglycemia: a score > 7 suggests a dumping and a score <4 suggests another diagnosis.

    Complementary questions regarding timing of dumping (<30 min or >1h30) will be asked if Sigstad score >7.

  15. Change of food choices and preferences assessed by the Leeds Food Preference Questionnaire (LFPQ) score.

    Time frame: from baseline to 24 months after surgery

    The Leeds Food Preference Questionnaire provides measures of different components of food preference and food reward. Participants are presented with an array of pictures of individual food items common in the diet. Foods in the array are chosen by the experimenter from a validated database to be either predominantly high (>50% energy) or low (<20% energy) in fat but similar in familiarity, protein content, sweet or non-sweet taste and palatability. Outcome measured are explicit Liking, explicit wanting, implicit wanting and food choice.

    Scores for explicit liking and explicit wanting range from 0-100 with a typical mean (±S.D.) of 60±18 Scores for Food Choice range from 0-48 and have a typical mean of 24±10 or for the appeal bias range from -48-48 with a typical mean of -5±15.

    Scores for Implicit Wanting typically range from -100-100 (due to RT there is no fixed min-max value) and have a typical mean of ±10±25 or for the appeal bias a typical mean of -10±30.

  16. Change of physical activity assessed by the International Physical Activity Index (IPAQ) score.

    Time frame: from baseline to 24 months after surgery

    The International Physical Activity Questionnaire assesses the types of intensity of physical activity and sitting time that people do as part of their daily lives to estimate total physical activity in MET-min/week and time spent sitting.

Sponsors and collaborators

Lead sponsor

University Hospital, Lille

Other

Collaborators

  • Ministry of Health, France

Registry information

Official study title

Prospective Multicentric Randomized Trial Comparing the Efficacy and Safety of Sleeve Gastrectomy With Transit Bipartition (SG+TB) Versus Roux-en-Y Gastric Bypass (RYGB)

Acronym: BIPASS

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Jun 7, 2021
Registry last updated
Feb 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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