search
Back to results

Comparing 150cm OAGB With 150cm Biliopancreatic Limb RYGB. A Non-inferiority Trial (Roux-en-WHY?)

Primary Purpose

Bariatric Surgery Candidate, Obesity, Obesity, Morbid

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
OAGB
RYGB
Sponsored by
Flevoziekenhuis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bariatric Surgery Candidate

Eligibility Criteria

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

Inclusion Criteria:

  • body-mass index (BMI) of 40 kg/m2 or higher, or 35 kg/m2 or higher with the presence of at least one comorbidity (type 2 diabetes, high blood pressure, obstructive sleep apnoea, dyslipidaemia, osteoarthritis of the hip or knee)
  • a positive evaluation by our BMDT

Exclusion Criteria:

  • Presence of H. Pylori, resistant to eradication therapy
  • chronic diarrhoea
  • history of previous bariatric or extensive abdominal surgery

Sites / Locations

  • FlevoziekenhuisRecruiting
  • OLVG

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

OAGB

RYGB

Arm Description

149 patients receiving one anastomosis gastric bypass (OAGB) with a Biliopancreatic-limb of 150cm

149 patients receiving Roux-en-Y gastric bypass (RYGB) with a Biliopancreatic-limb of 150cm

Outcomes

Primary Outcome Measures

Percentage excess BMI loss at 2 years (%EBMIL)
Percentage excess BMI loss after 2 years of follow-up

Secondary Outcome Measures

Full Information

First Posted
October 6, 2020
Last Updated
February 14, 2023
Sponsor
Flevoziekenhuis
search

1. Study Identification

Unique Protocol Identification Number
NCT04852198
Brief Title
Comparing 150cm OAGB With 150cm Biliopancreatic Limb RYGB. A Non-inferiority Trial
Acronym
Roux-en-WHY?
Official Title
A Study on Safety and Efficacy Comparing 150cm One Anastomosis Gastric Bypass With 150cm Biliopancreatic Limb Roux-en-Y Gastric Bypass (Roux-en-WHY?): An Open Label, Multicentre Non-inferiority Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 13, 2021 (Actual)
Primary Completion Date
June 13, 2027 (Anticipated)
Study Completion Date
November 1, 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Flevoziekenhuis

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to assess the safety and efficiency of OAGB compared to RYGB
Detailed Description
Rationale: to compare two different types of gastric bypass operations on surgical outcome. Objective: to compare two established procedures in order to find the optimal procedure in terms of weight loss and metabolic control that is associated with the fewest side-effects and complications, and decreased invasiveness. Study design: A multicentre, open label, non-inferiority randomized controlled trial Study population: Patients are eligible for inclusion if their body-mass index (BMI) was 40 kg/m2 or higher, or 35 kg/m2 or higher with the presence of at least one comorbidity (type 2 diabetes, high blood pressure, obstructive sleep apnoea, dyslipidaemia, osteoarthritis of the hip or knee) and a positive evaluation by our bariatric multidisciplinary team (BMDT) and are aged 18-65. Intervention: Group 1: One Anastomosis Gastric Bypass with 150cm biliopancreatic limb. Group 2: Roux-en-Y gastric bypass with biliopancreatic limb of 150cm and 75cm alimentary limb. Main study parameters/endpoints: Primary endpoint: % Excess BMI loss at two years Secondary endpoints: Metabolic status Nutritional status Comorbidity remission QOL Complications or serious adverse events (SAE's)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bariatric Surgery Candidate, Obesity, Obesity, Morbid

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial with 2 groups
Masking
None (Open Label)
Allocation
Randomized
Enrollment
298 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
OAGB
Arm Type
Active Comparator
Arm Description
149 patients receiving one anastomosis gastric bypass (OAGB) with a Biliopancreatic-limb of 150cm
Arm Title
RYGB
Arm Type
Active Comparator
Arm Description
149 patients receiving Roux-en-Y gastric bypass (RYGB) with a Biliopancreatic-limb of 150cm
Intervention Type
Procedure
Intervention Name(s)
OAGB
Other Intervention Name(s)
Mini gastric bypass, Omega loop gastric bypass
Intervention Description
Simplified gastric bypass procedure
Intervention Type
Procedure
Intervention Name(s)
RYGB
Intervention Description
Roux-en-Y gastric bypass. Standard procedure in the Netherlands
Primary Outcome Measure Information:
Title
Percentage excess BMI loss at 2 years (%EBMIL)
Description
Percentage excess BMI loss after 2 years of follow-up
Time Frame
2 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: body-mass index (BMI) of 40 kg/m2 or higher, or 35 kg/m2 or higher with the presence of at least one comorbidity (type 2 diabetes, high blood pressure, obstructive sleep apnoea, dyslipidaemia, osteoarthritis of the hip or knee) a positive evaluation by our BMDT Exclusion Criteria: Presence of H. Pylori, resistant to eradication therapy chronic diarrhoea history of previous bariatric or extensive abdominal surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stef JM Smeets, MD PhD
Phone
0031368688888
Email
ssmeets@flevoziekenhuis.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Floris Bruinsma, Student
Phone
0031368688888
Email
fbruinsma@flevoziekenhuis.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stef JM Smeets, MD PhD
Organizational Affiliation
Flevoziekenhuis
Official's Role
Principal Investigator
Facility Information:
Facility Name
Flevoziekenhuis
City
Almere
ZIP/Postal Code
1315RA
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Floris Bruinsma, MD
Email
florisbruinsma@live.nl
First Name & Middle Initial & Last Name & Degree
Christel Boons, PhD
Email
wetenschapsbureau@flevoziekenhuis.nl
Facility Name
OLVG
City
Amsterdam
ZIP/Postal Code
1061AE
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Phillip Dijkhorst, MD
Email
p.j.dijkhorst@olvg.nl
First Name & Middle Initial & Last Name & Degree
Robin Debi
Email
r.a.debi@olvg.nl

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Comparing 150cm OAGB With 150cm Biliopancreatic Limb RYGB. A Non-inferiority Trial

We'll reach out to this number within 24 hrs