Banded Versus Non-banded Roux-en-y Gastric Bypass

Status Active, not recruiting

Clinical Trial Summary

Clinical Trial Description

A Roux-en-Y Gastric Bypass (RYGB) is on the long term not always successful in every patient because weight regain can occur. An intervention to prevent weight regain in the future is to place a silicone band (non-adjustable) around the pouch of the RYGB (Banded-RYGB: BRYGB) which increases weight loss and decreases weight regain on the longer term. The question is whether primary application of a banded bypass gives a greater weight loss and / or prevent weight regain in the future versus a standard RYGB.

The Study design is a prospective, randomized, single center study.

Study population: patients who qualify for a RYGB are eligible to participate. The primary RYGB patients may participate if there is a BMI of 35 kg / m2 with a morbidly obesity-related comorbidity or a BMI of 40kg / m2 or higher.

Intervention: The standard RYGB with a vertical pouch over a 40 french feeding tube with a volume of 30-50 ml, is compared with a banded-RYGB (BRYGB) ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02545647
Study type	Interventional
Source	Rijnstate Hospital
Contact
Status	Active, not recruiting
Phase	N/A
Start date	September 2015
Completion date	September 2019

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Banded Versus Non-banded Roux-en-y Gastric Bypass — Bandolera

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms