RYGB AL 150cm BPL 100cm vs RYGB AL 100cc BPL 150cm
Primary Purpose
Weight Loss
Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
AL 150 BPL100
AL 100 BPL 150
Sponsored by

About this trial
This is an interventional treatment trial for Weight Loss
Eligibility Criteria
Inclusion Criteria:
- BMI > 40 Kg/m2
- BMI > 35 Kg/m2, associated with obesity-related comorbidities
- Patients undergoing Roux-en-Y gastric bypass as bariatric procedure
Exclusion Criteria:
- Patients undergoing Roux-en-Y gastric bypass as revisional procedure
- Patients lost to follow-up
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
AL150 BPL100
AL100 BPL150
Arm Description
Roux-en-Y gastric bypass with 150cm of alimentary limb and 100cm of biliopancreatic limb
Roux-en-Y gastric bypass with 100cm of alimentary limb and 150cm of biliopancreatic limb
Outcomes
Primary Outcome Measures
Weight loss
Weight loss will be assessed 1 year after surgery
Secondary Outcome Measures
Full Information
NCT ID
NCT03838276
First Posted
February 9, 2019
Last Updated
February 9, 2019
Sponsor
Hospital General Universitario Elche
1. Study Identification
Unique Protocol Identification Number
NCT03838276
Brief Title
RYGB AL 150cm BPL 100cm vs RYGB AL 100cc BPL 150cm
Official Title
Ponderal Outcomes After Roux-en-Y Gastric Bypass With Alimentary Limb (AL) of 150cm and Biliopancreatic Limb (BPL) of 100cm vs AL 100cm and BPL 150cm
Study Type
Interventional
2. Study Status
Record Verification Date
February 2019
Overall Recruitment Status
Unknown status
Study Start Date
February 15, 2019 (Anticipated)
Primary Completion Date
February 15, 2020 (Anticipated)
Study Completion Date
February 15, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital General Universitario Elche
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A Roux-en-Y gastric bypass will be performed in all the cases. Patients will be randomized according the limb lengths:
Group 1: Alimentary limb (AL) 150cm and biliopancreatic limb (BPL) 100cm
Group 2: AL 100cm and BPL 150cm
Weight loss will be evaluated 1 year after surgery
Detailed Description
A Roux-en-Y gastric bypass will be performed in all the cases. Patients will be randomized according the limb lengths:
Group 1: Alimentary limb 150cm and biliopancreatic limb 100cm
Group 2: Alimentary limb 100cm and biliopancreatic limb 150cm
Weight loss will be evaluated 1 year after surgery
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weight Loss
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
AL150 BPL100
Arm Type
Active Comparator
Arm Description
Roux-en-Y gastric bypass with 150cm of alimentary limb and 100cm of biliopancreatic limb
Arm Title
AL100 BPL150
Arm Type
Experimental
Arm Description
Roux-en-Y gastric bypass with 100cm of alimentary limb and 150cm of biliopancreatic limb
Intervention Type
Procedure
Intervention Name(s)
AL 150 BPL100
Intervention Description
Roux-en-Y gastric bypass with 150cm of alimentary limb and 100cm of biliopancreatic limb
Intervention Type
Procedure
Intervention Name(s)
AL 100 BPL 150
Intervention Description
Roux-en-Y gastric bypass with 100cm of alimentary limb and 150cm of biliopancreatic limb
Primary Outcome Measure Information:
Title
Weight loss
Description
Weight loss will be assessed 1 year after surgery
Time Frame
1 year after surgery
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:
BMI > 40 Kg/m2
BMI > 35 Kg/m2, associated with obesity-related comorbidities
Patients undergoing Roux-en-Y gastric bypass as bariatric procedure
Exclusion Criteria:
Patients undergoing Roux-en-Y gastric bypass as revisional procedure
Patients lost to follow-up
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jaime Ruiz-Tovar
Phone
630534808
Email
jruiztovar@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Lucas Rivalletto
Phone
+34654987159
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Santiago de Battista
Organizational Affiliation
Hospital La PLata
Official's Role
Study Chair
12. IPD Sharing Statement
Learn more about this trial
RYGB AL 150cm BPL 100cm vs RYGB AL 100cc BPL 150cm
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