Actively Recruiting
Laparoscopic Single Anastomosis Sleeve Ileal Bypass Versus Laparoscopic Sleeve Gastrectomy for Morbid Obesity
Led by Oslo University Hospital · Updated on 2024-04-03
220
Participants Needed
2
Research Sites
406 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study will compare two bariatric surgical interventions in terms of weight loss, gastroesophageal reflux, and effects on obesity-related comorbid conditions in morbidly obese patients.
CONDITIONS
Official Title
Laparoscopic Single Anastomosis Sleeve Ileal Bypass Versus Laparoscopic Sleeve Gastrectomy for Morbid Obesity
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Morbid obesity at referral for bariatric surgery (BMI 235 kg/m2 with obesity-related comorbid conditions or 240 kg/m2 with or without such comorbidities)
- Age 20 to 60 years
- Previous failed attempts of weight loss
- Norwegian speaking patients
You will not qualify if you...
- BMI 255 kg/m2
- History of major abdominal or bariatric surgery (excluding appendectomy, cholecystectomy, and cesarean section)
- Established disabling cardiopulmonary disease
- Ongoing treatment for cancer
- Long-term steroid use
- Conditions believed to be associated with poor adherence after surgery
- Previous or current daily gastroesophageal reflux symptoms or daily use of antireflux medication
- Preoperative manometry identifying hiatal hernia 254 cm in axial length
- Preoperative upper endoscopy showing esophagitis grade C or D, peptic stricture, Barrett's esophagus, or esophageal carcinoma
- Achalasia
- Pregnancy
AI-Screening
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Trial Site Locations
Total: 2 locations
1
The Morbid Obesity Center, Vestfold Hospital Trust
Tønsberg, Vestfold, Norway, 3103
Not Yet Recruiting
2
Oslo University Hospital
Oslo, Norway, 4950
Actively Recruiting
Research Team
H
Helene M Haug, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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