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Laparoscopic Gastric Bypass Versus Laparoscopic Banded Gastric Bypass Randomized Prospective Clinical Trial (LGB-vs-LbGB)

Primary Purpose

Morbid Obesity, Weight Loss, Postoperative Complications

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Banded (with polypropylene mesh) gastric bypass
Gastric bypass
Sponsored by
Puerta de Hierro University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Morbid Obesity focused on measuring banded gastric bypass, weight loss

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • criteria for bariatric surgery published in 1991 for the National Institutes of Health of the USA.
  • Body mass index (BMI)> 40 and <55 kg/m2
  • Obesity for more than 5 years of evolution
  • Fail in medical supervised weight loss program
  • patient knowing of the mechanism of weight loss after surgery and agreement to collaborate with medical recommendations, diet, medical treatment, as well as the visit established in the follow up program
  • patient accepting that surgery objective is not to achieve the ideal weight.
  • signed specific informed consent
  • women will agree in avoid gestation during one year after surgery

Exclusion Criteria:

  • Patients unable to sign the informed consent form because of a mental disorder.
  • endocrine diseases causing obesity
  • unstable mental disorder, evaluated for a psychiatry MD.
  • high anesthetic risk making surgery too risky.
  • Malignant neoplasm
  • Inflammatory bowel disease
  • Severe liver disease
  • Digestive disease that makes unwise the bypass technique (mainly gastric illness that may required upper endoscopy for control)
  • abdominal wall hernias
  • Symptomatic biliary pathology that requires cholechistectomy at the same time of the bariatric surgery
  • any known pathology that requieres or recomend simultaneous surgery at the time of the bariatric surgery.

Sites / Locations

  • Servicio de Cirugía General. Hospital Universitario Puerta de Hierro Majadahonda

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Banded Gastric Bypass

Gastric Bypass.

Arm Description

The patient will have done a laparoscopic Roux-en-Y banded (with polypropylene mesh) gastric bypass at the time of the surgical procedure.

The patient will have done a Laparoscopic Roux-en-Y gastric bypass at the time of the surgical procedure

Outcomes

Primary Outcome Measures

Change from operation date, in excess weight loss at 10 years
% of excess weight loss at 10 years
Postoperative complications at 10 years
Number of participants with adverse events (surgical complications) and/or abnormal Laboratory values that are related to treatment

Secondary Outcome Measures

Excess weight loss at 5 years
% of excess weight loss at 5 years
Total Hospital cost at 3 months
Total hospital expenses during admission for the surgery and 3 months after the operation.
Postoperative complications 1 year
Number of participants with adverse events (surgical complications)
Postoperative complications 2 years
Number of participants with adverse events (surgical complications)
Postoperative complications 3 years
Number of participants with adverse events (surgical complications)
Postoperative complications 5 years
Number of participants with adverse events (surgical complications)

Full Information

First Posted
September 28, 2016
Last Updated
April 18, 2020
Sponsor
Puerta de Hierro University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02939664
Brief Title
Laparoscopic Gastric Bypass Versus Laparoscopic Banded Gastric Bypass Randomized Prospective Clinical Trial
Acronym
LGB-vs-LbGB
Official Title
Laparoscopic Gastric Bypass Versus Laparoscopic Banded Gastric Bypass, a Randomized Prospective Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Enrolling by invitation
Study Start Date
April 2016 (undefined)
Primary Completion Date
January 2034 (Anticipated)
Study Completion Date
January 2034 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Puerta de Hierro University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study try to identify differences in length of operation, weight loss and complications, between two different bariatric surgical techniques, the laparoscopic Roux-en-Y gastric bypass and the laparoscopic Roux-en-Y banded gastric bypass. The study will be conducted in a Spanish public health system hospital. The patients of the trial will have the preoperative studies, hospital treatment during the admission, postoperative treatment and follow up as any other patient included in the hospital bariatric surgery program. The study cases will have placed around the gastric pouch a band of polypropylene mesh, and will be randomly choose between the participants. Patients will be randomized in a 5/3 (study/control) ratio.
Detailed Description
One group of patients of the study will have done the simplified laparoscopic gastric bypass, with a vertical gastric pouch of about 20 ml, a 150 cm Roux-en-Y limb constructed in an antegastric antecolic fashion, and a biliary limb of 100 cm. Anastomosis will be done with endoscopic surgical linear stapler, closing the apertures with continuous absorbable running sutures. The Petersen space and the mesenteric defect will be closed with non-absorbable sutures. The other group of patients will have performed the laparoscopic Roux-en-Y banded gastric bypass. This technique is identical to the one performed in the other group, but differs in that a polypropylene mesh (10x65 mm) is placed 15 mm proximal to the anastomosis around the gastric pouch, and the gastric pouch is about 15 mm longer. The investigators randomly assigned 50 patients to the study group (Laparoscopic Roux-en-Y banded gastric bypass) and 30 to the control group (Laparoscopic Roux-en-Y gastric bypass) , n=80, and were also blinded to the surgeon until surgery. One of the methods is basically the same than the other, but for the placement of the polypropylene mesh around the gastric pouch above the anastomosis, and patient series with Laparoscopic Roux-en-Y banded gastric bypass showed long term better weight loss than other series with not banded gastric bypass, thus it is expected a difference in long term weight loss between groups. Fisher Test will be used for the statistical analysis, assuming a risk of 0.05 and a statistical power of 90%. Sample size is calculated considering bibliographic long term weight loss in both groups, which is 82% in the banded group versus 63% in the not banded group. Thus sample size (n): 67, and adjust by loss sample size: 79 (10% expected loss ratio), not being necessary a 1: 1 ratio between cases and controls and requiring no more than 25 controls, A sample size of 50 cases and 30 controls, total n = 80, will be used. The method of randomization was concealed envelopes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Morbid Obesity, Weight Loss, Postoperative Complications
Keywords
banded gastric bypass, weight loss

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Banded Gastric Bypass
Arm Type
Active Comparator
Arm Description
The patient will have done a laparoscopic Roux-en-Y banded (with polypropylene mesh) gastric bypass at the time of the surgical procedure.
Arm Title
Gastric Bypass.
Arm Type
Active Comparator
Arm Description
The patient will have done a Laparoscopic Roux-en-Y gastric bypass at the time of the surgical procedure
Intervention Type
Device
Intervention Name(s)
Banded (with polypropylene mesh) gastric bypass
Other Intervention Name(s)
Laparoscopic banded gastric bypass, Laparoscopic Roux-en-Y banded gastric bypass, Laparoscopic Banded Roux-en-Y gastric bypass
Intervention Description
The patient will be submitted to a Laparoscopic Roux-en-Y banded gastric bypass at the time of the operation, with a polypropylene mesh around the gastric pouch.
Intervention Type
Procedure
Intervention Name(s)
Gastric bypass
Other Intervention Name(s)
Laparoscopic Gastric bypass
Intervention Description
In this case a simplified conventional gastric bypass will be performed
Primary Outcome Measure Information:
Title
Change from operation date, in excess weight loss at 10 years
Description
% of excess weight loss at 10 years
Time Frame
10 years
Title
Postoperative complications at 10 years
Description
Number of participants with adverse events (surgical complications) and/or abnormal Laboratory values that are related to treatment
Time Frame
10 years
Secondary Outcome Measure Information:
Title
Excess weight loss at 5 years
Description
% of excess weight loss at 5 years
Time Frame
5 years
Title
Total Hospital cost at 3 months
Description
Total hospital expenses during admission for the surgery and 3 months after the operation.
Time Frame
up to 3 months
Title
Postoperative complications 1 year
Description
Number of participants with adverse events (surgical complications)
Time Frame
1 year
Title
Postoperative complications 2 years
Description
Number of participants with adverse events (surgical complications)
Time Frame
2 years
Title
Postoperative complications 3 years
Description
Number of participants with adverse events (surgical complications)
Time Frame
3 years
Title
Postoperative complications 5 years
Description
Number of participants with adverse events (surgical complications)
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: criteria for bariatric surgery published in 1991 for the National Institutes of Health of the USA. Body mass index (BMI)> 40 and <55 kg/m2 Obesity for more than 5 years of evolution Fail in medical supervised weight loss program patient knowing of the mechanism of weight loss after surgery and agreement to collaborate with medical recommendations, diet, medical treatment, as well as the visit established in the follow up program patient accepting that surgery objective is not to achieve the ideal weight. signed specific informed consent women will agree in avoid gestation during one year after surgery Exclusion Criteria: Patients unable to sign the informed consent form because of a mental disorder. endocrine diseases causing obesity unstable mental disorder, evaluated for a psychiatry MD. high anesthetic risk making surgery too risky. Malignant neoplasm Inflammatory bowel disease Severe liver disease Digestive disease that makes unwise the bypass technique (mainly gastric illness that may required upper endoscopy for control) abdominal wall hernias Symptomatic biliary pathology that requires cholechistectomy at the same time of the bariatric surgery any known pathology that requieres or recomend simultaneous surgery at the time of the bariatric surgery.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Miguel J Garcia-Oria, MD PhD FACS
Organizational Affiliation
General Surgery Department. Hospital Universitario Puerta de Hierro
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Miguel J Garcia-Oria, MD PhD
Organizational Affiliation
Servicio de Cirugía General. Hospital Universitario Puerta de Hierro Majadahonda
Official's Role
Study Director
Facility Information:
Facility Name
Servicio de Cirugía General. Hospital Universitario Puerta de Hierro Majadahonda
City
Majadahonda
State/Province
Madrid
ZIP/Postal Code
28222
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
We will publish the results of the study in a surgical journal
Citations:
PubMed Identifier
18226982
Citation
Arceo-Olaiz R, Espana-Gomez MN, Montalvo-Hernandez J, Velazquez-Fernandez D, Pantoja JP, Herrera MF. Maximal weight loss after banded and unbanded laparoscopic Roux-en-Y gastric bypass: a randomized controlled trial. Surg Obes Relat Dis. 2008 Jul-Aug;4(4):507-11. doi: 10.1016/j.soard.2007.11.006. Epub 2008 Jan 28.
Results Reference
background
PubMed Identifier
17544335
Citation
Bessler M, Daud A, Kim T, DiGiorgi M. Prospective randomized trial of banded versus nonbanded gastric bypass for the super obese: early results. Surg Obes Relat Dis. 2007 Jul-Aug;3(4):480-4; discussion 484-5. doi: 10.1016/j.soard.2007.01.010. Epub 2007 Jun 4.
Results Reference
background
PubMed Identifier
25001288
Citation
Buchwald H, Buchwald JN, McGlennon TW. Systematic review and meta-analysis of medium-term outcomes after banded Roux-en-Y gastric bypass. Obes Surg. 2014 Sep;24(9):1536-51. doi: 10.1007/s11695-014-1311-1.
Results Reference
background
PubMed Identifier
11918873
Citation
Capella JF, Capella RF. An assessment of vertical banded gastroplasty-Roux-en-Y gastric bypass for the treatment of morbid obesity. Am J Surg. 2002 Feb;183(2):117-23. doi: 10.1016/s0002-9610(01)00871-6.
Results Reference
background
PubMed Identifier
8554155
Citation
Capella JF, Capella RF. The weight reduction operation of choice: vertical banded gastroplasty or gastric bypass? Am J Surg. 1996 Jan;171(1):74-9. doi: 10.1016/S0002-9610(99)80077-4.
Results Reference
background
PubMed Identifier
24968745
Citation
Mahawar KK, Parikh C, Carr WR, Jennings N, Balupuri S, Small PK. Primary banded Roux-en-Y gastric bypass: a systematic review. Obes Surg. 2014 Oct;24(10):1771-92. doi: 10.1007/s11695-014-1346-3.
Results Reference
background
PubMed Identifier
26314349
Citation
Rasera I Jr, Coelho TH, Ravelli MN, Oliveira MR, Leite CV, Naresse LE, Henry MA. A Comparative, Prospective and Randomized Evaluation of Roux-en-Y Gastric Bypass With and Without the Silastic Ring: A 2-Year Follow Up Preliminary Report on Weight Loss and Quality of Life. Obes Surg. 2016 Apr;26(4):762-8. doi: 10.1007/s11695-015-1851-z.
Results Reference
background
PubMed Identifier
23260801
Citation
Zarate X, Arceo-Olaiz R, Montalvo Hernandez J, Garcia-Garcia E, Pablo Pantoja J, Herrera MF. Long-term results of a randomized trial comparing banded versus standard laparoscopic Roux-en-Y gastric bypass. Surg Obes Relat Dis. 2013 May-Jun;9(3):395-7. doi: 10.1016/j.soard.2012.09.009. Epub 2012 Oct 3.
Results Reference
background

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Laparoscopic Gastric Bypass Versus Laparoscopic Banded Gastric Bypass Randomized Prospective Clinical Trial

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