Skip to main content
OpenTrials
Recruiting

NCT Number: NCT04852198

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

The purpose of this study is to assess the safety and efficiency of OAGB compared to RYGB

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Flevoziekenhuis, Almere Stad, Netherlands

Loading trial locations.

About this study

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)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

OAGB

Procedure

Simplified gastric bypass procedure

Other names: Mini gastric bypass, Omega loop gastric bypass

RYGB

Procedure

Roux-en-Y gastric bypass. Standard procedure in the Netherlands

Primary outcomes

  1. Percentage excess BMI loss at 2 years (%EBMIL)

    Time frame: 2 years

    Percentage excess BMI loss after 2 years of follow-up

Study contacts

Contact information is provided by the study sponsor or research team.

Floris Bruinsma, Student

CONTACT

[email protected]

0031368688888

Stef JM Smeets, MD PhD

CONTACT

[email protected]

0031368688888

Sponsors and collaborators

Lead sponsor

Flevoziekenhuis

Other

Registry information

Official study 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

Acronym: Roux-en-WHY?

Important dates

Study start
2021
Primary completion
2027
Study completion
2029
First posted
Apr 21, 2021
Registry last updated
Apr 23, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.