A Comparison of the Bariatric Procedures that Are Performed in the Treatment of Super Morbid Obesity.
Kohei Uno, Yosuke Seki, Kazunori Kasama...
https://pubmed.ncbi.nlm.nih.gov/28451928/Actively Recruiting
Led by Chulalongkorn University · Updated on 2026-08-06
32
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are comparing two bariatric surgery techniques in people with super morbid obesity, specifically those with a BMI of 50-60 kgm2 who have not lost weight despite medical therapy and exercise. The study evaluates hormonal responses and the incidence of post-bariatric hypoglycemia after laparoscopic Roux-en-Y gastric bypass LRYGB and laparoscopic sleeve gastrectomy with duodenojejunal bypass LSG-DJB. This comparison aims to clarify the mechanisms behind weight loss and postprandial blood sugar changes following these surgeries. The study involves two surgical procedures. LSG-DJB reduces stomach volume to about 80-150 mL and reroutes part of the small intestine to create a bypass, while LRYGB reduces stomach volume to about 15-50 mL and connects the jejunum directly to the gastric pouch with a different bypass configuration. Participants are randomly assigned to receive one of the two procedures, with LRYGB being the standard approach and LSG-DJB as the experimental technique. Participants will be followed for 6 to 24 months after surgery, during which researchers will assess hormonal responses including GLP-1, GIP, glucagon, and insulin levels. They will also monitor the occurrence of post-bariatric hypoglycemia and other outcomes related to weight loss and metabolic health. This extended monitoring helps understand the benefits and risks of each surgery over time.
CONDITIONS
Comparison of Hormonal Response to a Mixed-Meal Tolerance Test After Laparoscopic Roux-en-Y Gastric Bypass Versus Laparoscopic Sleeve Gastrectomy With Duodenojejunal Bypass in Patients With Super Morbid Obesity
P
Primploy Greeviroj, M.D., M.Sc.
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Chulalongkorn University
Lead Sponsor
Ratchadapiseksompotch Research Fund
Collaborating Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 6 to 24 months
Participants undergo one of two bariatric surgeries: laparoscopic sleeve gastrectomy with duodenojejunal bypass or laparoscopic Roux-en-Y gastric bypass.
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/29370995/Chulalongkorn University
Lead Sponsor
Ratchadapiseksompotch Research Fund
Collaborating Sponsor