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Laparoscopic Roux-en-Y Gastric Bypass Versus Laparoscopic One Anastomosis Gastric Bypass (OAGB-vs-LRYGB)

Primary Purpose

Morbid Obesity, Postoperative Complications, Weight Loss

Status
Active
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Minigastric 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 gastric bypass, hospital charges, mini gastric bypass

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.
  • age between 18-65 years-old.
  • BMI between 40-50 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
  • Gastroesophageal reflux disease (GERD) with endoscopic esophagitis

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

Minigastric bypass

Gastric bypass

Arm Description

Intervention(s): The patient will have done a Laparoscopic one anastomosis gastric bypass (minigastric bypass) at the time of the surgical procedure.

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

Outcomes

Primary Outcome Measures

Hospital Cost in euros
Total hospital expenses during admission for the surgery
Length of operation in minutes
Duration of the surgical procedure

Secondary Outcome Measures

weight loss in kilograms
weight of the patient at clinics, 3 months after surgery
weight loss in kilograms
weight of the patient at clinics, 6 months after surgery
weight loss in kilograms
weight of the patient at clinics, 9 months after surgery
weight loss in kilograms
weight of the patient at clinics, 12 months after surgery
weight loss in kilograms
weight of the patient at clinics, 18 months after surgery
weight loss in kilograms
weight of the patient at clinics, 24 months after surgery
weight loss in kilograms
weight of the patient at clinics, 3 years after surgery
weight loss in kilograms
weight of the patient at clinics, 4 years after surgery
weight loss in kilograms
weight of the patient at clinics, 5 years after surgery

Full Information

First Posted
May 16, 2016
Last Updated
April 18, 2020
Sponsor
Puerta de Hierro University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02779322
Brief Title
Laparoscopic Roux-en-Y Gastric Bypass Versus Laparoscopic One Anastomosis Gastric Bypass
Acronym
OAGB-vs-LRYGB
Official Title
Prospective Randomized Controlled Clinical Trial: Laparoscopic Roux-en-Y Gastric Bypass Versus Laparoscopic One Anastomosis Gastric Bypass
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 2015 (undefined)
Primary Completion Date
November 2019 (Actual)
Study Completion Date
June 2025 (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 cost, length of operation and results between two different bariatric surgical techniques, the laparoscopic Roux-en-Y gastric bypass and the Single anastomosis laparoscopic 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. No new methods are applied other than randomly choose the surgical technique. Patients will be randomized in a 1:1 ratio to each group.
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 single anastomosis gastric bypass, also known as the Minigastric bypass (MGB), which have a vertical gastric pouch about 100-150 ml, and an end to side gastro-jejunal anastomosis at 200 cm from Treitz angle. The anastomosis will be done with endoscopic surgical linear stapler, closing the aperture with continuous absorbable running sutures.The Petersen space will be also close with non-absorbable sutures. The investigators randomly assigned 10 patients to each group, n=20. Considering that one of the methods is basically the same than the other, but for the Roux-en-Y construction, it is expected a clear difference in operating room (OR) time, between groups. Fisher Test, will be used for the statistical analysis, assuming a risk of 0.05 and a statistical power of 90%, and Mann-Whitney test for quantitative parameters. Once patients were included in the study, they were randomized in a 1:1 ratio to the conventional laparoscopic gastric bypass group or the single-anastomosis laparoscopic gastric bypass (Mini gastric bypass) group and were also blinded to the surgeon until surgery. 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, Postoperative Complications, Weight Loss
Keywords
gastric bypass, hospital charges, mini gastric bypass

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Minigastric bypass
Arm Type
Active Comparator
Arm Description
Intervention(s): The patient will have done a Laparoscopic one anastomosis gastric bypass (minigastric bypass) at the time of the surgical procedure.
Arm Title
Gastric bypass
Arm Type
Active Comparator
Arm Description
The patient will have a Laparoscopic Roux-en-Y gastric bypass at the time of the surgical procedure
Intervention Type
Procedure
Intervention Name(s)
Minigastric bypass
Other Intervention Name(s)
Single or One anastomosis gastric bypass
Intervention Description
The patient will be submitted to a minigastric bypass at the time of the operation
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
Hospital Cost in euros
Description
Total hospital expenses during admission for the surgery
Time Frame
up to 3 months
Title
Length of operation in minutes
Description
Duration of the surgical procedure
Time Frame
1 day
Secondary Outcome Measure Information:
Title
weight loss in kilograms
Description
weight of the patient at clinics, 3 months after surgery
Time Frame
3 months
Title
weight loss in kilograms
Description
weight of the patient at clinics, 6 months after surgery
Time Frame
6 months
Title
weight loss in kilograms
Description
weight of the patient at clinics, 9 months after surgery
Time Frame
9 months
Title
weight loss in kilograms
Description
weight of the patient at clinics, 12 months after surgery
Time Frame
12 months
Title
weight loss in kilograms
Description
weight of the patient at clinics, 18 months after surgery
Time Frame
18 months
Title
weight loss in kilograms
Description
weight of the patient at clinics, 24 months after surgery
Time Frame
24 months
Title
weight loss in kilograms
Description
weight of the patient at clinics, 3 years after surgery
Time Frame
3 years
Title
weight loss in kilograms
Description
weight of the patient at clinics, 4 years after surgery
Time Frame
4 years
Title
weight loss in kilograms
Description
weight of the patient at clinics, 5 years after surgery
Time Frame
5 years
Other Pre-specified Outcome Measures:
Title
Number of Participants With Abnormal Laboratory Values and/or Adverse Events That Are Related to Treatment
Description
Record of any adverse event and/or abnormal laboratory values in relation with the operation performed since the day of the operation to the study completion.
Time Frame
through study completion an average of 5 year

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. age between 18-65 years-old. BMI between 40-50 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 Gastroesophageal reflux disease (GERD) with endoscopic esophagitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Miguel J Garcia-Oria, MD PhD FACS
Organizational Affiliation
Unidad Cirugia Obesidad y Metabolica Hospital Puerta de Hierro
Official's Role
Study Chair
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
The plan is to publish the results of our study in a scientific journal when it be completed, not to publish the individual patient data, just the global data comparing both groups of study.
Citations:
PubMed Identifier
23011462
Citation
Lee WJ, Ser KH, Lee YC, Tsou JJ, Chen SC, Chen JC. Laparoscopic Roux-en-Y vs. mini-gastric bypass for the treatment of morbid obesity: a 10-year experience. Obes Surg. 2012 Dec;22(12):1827-34. doi: 10.1007/s11695-012-0726-9.
Results Reference
background
PubMed Identifier
11433900
Citation
Rutledge R. The mini-gastric bypass: experience with the first 1,274 cases. Obes Surg. 2001 Jun;11(3):276-80. doi: 10.1381/096089201321336584.
Results Reference
background
PubMed Identifier
15973097
Citation
Lee WJ, Yu PJ, Wang W, Chen TC, Wei PL, Huang MT. Laparoscopic Roux-en-Y versus mini-gastric bypass for the treatment of morbid obesity: a prospective randomized controlled clinical trial. Ann Surg. 2005 Jul;242(1):20-8. doi: 10.1097/01.sla.0000167762.46568.98.
Results Reference
background
PubMed Identifier
25056233
Citation
Lee WJ, Lin YH. Single-anastomosis gastric bypass (SAGB): appraisal of clinical evidence. Obes Surg. 2014 Oct;24(10):1749-56. doi: 10.1007/s11695-014-1369-9.
Results Reference
background
PubMed Identifier
25661550
Citation
Piche ME, Auclair A, Harvey J, Marceau S, Poirier P. How to choose and use bariatric surgery in 2015. Can J Cardiol. 2015 Feb;31(2):153-66. doi: 10.1016/j.cjca.2014.12.014. Epub 2014 Dec 15.
Results Reference
background
PubMed Identifier
25409956
Citation
Ramos AC, Silva AC, Ramos MG, Canseco EG, Galvao-Neto Mdos P, Menezes Mde A, Galvao TD, Bastos EL. Simplified gastric bypass: 13 years of experience and 12,000 patients operated. Arq Bras Cir Dig. 2014;27 Suppl 1(Suppl 1):2-8. doi: 10.1590/s0102-6720201400s100002.
Results Reference
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Laparoscopic Roux-en-Y Gastric Bypass Versus Laparoscopic One Anastomosis Gastric Bypass

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