- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01806506
Randomized Comparison of Laparoscopic Sleeve Gastrectomy and Gastric Bypass for Morbid Obesity
October 8, 2018 updated by: Medical University of Warsaw
Randomized Clinical Trial Comparing Laparoscopic Sleeve Gastrectomy and Gastric Bypass for Morbid Obesity and Underlying Metabolic and Hormonal Abnormalities
Bariatric surgery is the most effective treatment for morbid obesity.
Roux-en-Y gastric bypass (RYGB) is a bariatric procedure with known safety and effectiveness.
Laparoscopic sleeve gastrectomy (LSG) is a newer procedure gaining popularity.
The aim of the study is to compare outcomes of these two surgical methods in terms of weight loss, improvement of common comorbidities of obesity and influence on metabolic and hormonal status.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Authors of the study believe that a more detailed head-to-head comparison of RYGB and LSG is necessary.
The former method is the established "gold standard" procedure with good outcomes reported in many studies.
However it is much more complex and the learning curve is longer.
The latter method was introduced as an initial procedure in superobese patients because of its relative simplicity.
It produced good outcomes in this population of superobese patients and surgeons in some centers started to use it as a primary bariatric procedure.
RYGB is a restrictive and partially malabsorptive procedure and it is believed to have additional benefits in patients with metabolic disorders such as type 2 diabetes and dyslipidemia.
Purely restrictive procedures such as LSG are theoretically less beneficial in this group of patients.
In the present study authors will look at weight loss as well as improvement in comorbidities and several biochemical parameters and indices to assess also metabolic action of these two procedures.
Study Type
Interventional
Enrollment (Actual)
72
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Warsaw, Poland, 02-097
- Department of General, Transplant and Liver Surgery, Public Central Teaching Hospital, Medical University of Warsaaw
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- BMI≥40 kg/m2
- BMI≥35 kg/m2 with at least one comorbidity associated with obesity
Exclusion Criteria:
- BMI > 60 kg/m2
- poorly controlled significant medical or psychiatric disorders
- active alcohol or substance abuse
- active duodenal/gastric ulcer disease
- difficult to treat gastro-esophageal reflux disease with a large hiatal hernia
- previous major gastrointestinal surgery
- diagnosed or suspected malignancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Laparoscopic sleeve gastrectomy
The group of morbidly obese patients assigned to laparoscopic sleeve gastrectomy.
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Laparoscopic sleeve gastrectomy (LSG) is a restrictive bariatric procedure.
LSG involves resection of a large part of the body and fundus of the stomach starting from the antrum up to the angle of His.
The remaining part of the stomach (the gastric sleeve) is calibrated with a 36 French bougie.
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Experimental: Roux-en-Y Gastric Bypass
The group of morbidly obese patients assigned to Roux-en-Y gastric bypass.
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Roux-en-Y gastric bypass (RYGB) is an intermediate (restrictive and malabsorptive) operation.
RYGB involves creation of a 15-20 mL gastric pouch that is anastomosed to a 100cm Roux limb created at 100cm from the ligament of Treitz.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Excess Weight Loss From Baseline
Time Frame: 12 months after surgery
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Weight loss measured as a percentage of excess weight lost is one of the most commonly used and accepted outcome measure in clinical trials evaluating bariatric surgery.
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12 months after surgery
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Number of Patients With Complications
Time Frame: 12 months after surgery
|
Complications are defined as any negative deviation from the normal postoperative course.
Complications of bariatric surgery include but are not limited to: gastrointestinal leak, intrabdominal bleeding, gastrointestinal bleeding, gastrointestinal stricture, gastrointestinal fistula, marginal ulceration, internal hernia, bowel obstruction, deep vein thrombosis, pulmonary embolism, wound infection, seroma, fascial dehiscence, abdominal hernia, gallstone formation, dehydration, nutritional deficiencies
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12 months after surgery
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Comorbidities Prevalence Changes
Time Frame: Evaluation at baseline and 1, 6 and 12 months after surgery
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Number of patients with comorbidities such as: type 2 diabetes mellitus, arterial hypertension, dyslipidemia, obstructive sleep apnea, degenerative arthritis, gallbladder disease, gastro-esophageal reflux disease.
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Evaluation at baseline and 1, 6 and 12 months after surgery
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Change in Weight From Baseline
Time Frame: Evaluation at baseline and 12 months after surgery
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Absolute weight loss (in kilograms) is evaluated.
It is one of the most commonly used and accepted outcome measures in clinical trials evaluating bariatric surgery.
It is more dependent on the initial weight of a study participant.
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Evaluation at baseline and 12 months after surgery
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Change in BMI From Baseline
Time Frame: Baseline and 12 months after surgery
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Assessment of Body Mass Index (weight divided by height in meters squared) change from baseline.
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Baseline and 12 months after surgery
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Plasma Total Cholesterol at 12 Months
Time Frame: 12 months after surgery
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Fasting plasma total cholesterol concentration in patients 12 months after surgery.
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12 months after surgery
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Plasma HDL at 12 Months
Time Frame: 12 months after surgery
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Fasting plasma high density lipoprotein (HDL) cholesterol concentration in patients 12 months after surgery.
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12 months after surgery
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Plasma LDL at 12 Months
Time Frame: 12 months after surgery
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Fasting plasma low density lipoprotein (LDL) cholesterol concentration in patients 12 months after surgery.
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12 months after surgery
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Plasma Triglycerides at 12 Months
Time Frame: 12 months after surgery
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Fasting plasma triglycerides concentration in patients 12 months after surgery.
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12 months after surgery
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Plasma Glucose at 12 Months
Time Frame: 12 months after surgery
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Fasting plasma glucose concentration in patients 12 months after surgery.
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12 months after surgery
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Plasma Insulin at 12 Months
Time Frame: 12 months after surgery
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Fasting plasma insulin concentration in patients 12 months after surgery.
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12 months after surgery
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Plasma C-peptide at 12 Months
Time Frame: 12 months after surgery
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Fasting plasma C-peptide concentration in patients 12 months after surgery.
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12 months after surgery
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HOMA Index at 12 Months
Time Frame: 12 months after surgery
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Insulin resistance (IR) measured with the homeostatic model assessment (HOMA) method.
In the published studies the HOMA model correlated with estimates using the reference euglycemic clamp method.
The following equation is used: HOMA-IR = (fasting plasma glucose concentration [mmol/L] x fasting plasma insulin concentration [miliunits/L])/22.5
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12 months after surgery
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HbA1c at 12 Months
Time Frame: 12 months after surgery
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The proportion of glycosylated hemoglobin (HbA1c) [%] is measured to assesses the average plasma glucose concentration and regulation.
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12 months after surgery
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Plasma CRP at 12 Months
Time Frame: 12 months after surgery
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C-reactive protein (CRP) is used as a marker of inflammation.
It may be also used in the assessment of heart disease risk.
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12 months after surgery
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Plasma Uric Acid at 12 Months
Time Frame: 12 months after surgery
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Hyperuricemia is associated with metabolic syndrome and obesity.
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12 months after surgery
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Plasma Ghrelin at 12 Months
Time Frame: 12 months after surgery
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Ghrelin is an appetite-stimulating hormone produced in the fundus of the stomach.
Its concentration may change after some bariatric procedures.
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12 months after surgery
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Plasma Leptin at 12 Months
Time Frame: 12 months after surgery
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Leptin is one of the adipose-derived hormones that causes inhibition of appetite.
Elevated leptin levels are associated with obesity, inflammation, metabolic syndrome and cardiovascular disease.
Weight loss leads to a decline in leptin concentrations.
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12 months after surgery
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Plasma Glucagon at 12 Months
Time Frame: 12 months after surgery
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Glucagon is synthesized and secreted from alpha cells of the pancreas.
It leads to elevation of the plasma glucose.
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12 months after surgery
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Plasma IGF-1 at 12 Months
Time Frame: 12 months after surgery
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Insulin like growth factor 1 (IGF-1) is similar in structure to insulin.
It has anabolic effects.
Its levels may be related to BMI and level of nutrition.
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12 months after surgery
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AST Level
Time Frame: 12 months
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12 months
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ALT Level
Time Frame: 12 months
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12 months
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INR
Time Frame: 12 months
|
12 months
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Albumin Level
Time Frame: 12 months
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12 months
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GGT Level
Time Frame: 12 months
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12 months
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ALP Level
Time Frame: 12 months
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12 months
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LDH Level
Time Frame: 12 months
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12 months
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Quality of Life Questionnaire Score
Time Frame: 12 months after surgery
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Quality of life questionnaire score at 12 months(WHO-Bref Quality of Life questionnaire)
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12 months after surgery
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Pulmonary Function Changes at 12 Months
Time Frame: Baseline and 12 months from surgery
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Spirometry and plethysmography results are used to assess pulmonary function before and after surgery.
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Baseline and 12 months from surgery
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Rafał Paluszkiewicz, Prof. MD,PhD, Medical University of Warsaw
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2008
Primary Completion (Actual)
March 1, 2012
Study Completion (Actual)
November 1, 2013
Study Registration Dates
First Submitted
January 31, 2013
First Submitted That Met QC Criteria
March 6, 2013
First Posted (Estimate)
March 7, 2013
Study Record Updates
Last Update Posted (Actual)
February 20, 2019
Last Update Submitted That Met QC Criteria
October 8, 2018
Last Verified
January 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KBN N N403 3882 33
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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