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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04834635
Other study ID # FundoRingOAGB
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 29, 2021
Est. completion date May 10, 2025

Study information

Verified date November 2023
Source The Society of Bariatric and Metabolic Surgeons of Kazakhstan
Contact Oral Ospanov, Professor
Phone +77015287734
Email bariatric.kz@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Currently, one anastomosis gastric bypass (OAGB) or mini-gastric bypass (MGB) is a common bariatric procedure for treating obesity. Weight gain after surgery is a big problem in bariatric practice. Therefore, adjustable bands and rings are used, for example, "FobiRing". But foreign material can cause complications - the erosion of the stomach wall. For this reason, surgeons avoid the use of various mechanical devices on living tissues. The greatest criticism is of the OAGB for the likelihood of biliary reflux. In case of reflux of bile into the esophagus after surgery, as a rule, a second operation is required with conversion OAGB to the Roux-en-Y method. In addition, along with obesity, gastroesophageal reflux disease (GERD) are steadily increasing world weight and antireflux surgery must be performed simultaneously with bariatric surgery in obese patients. In these cases, most often in bariatric practice, hiatus cruroraphy is performed, and less often fundoplication using the fundus of the excluded part of the stomach. We hypothesize that total fundoplication can not only treat GERD but also significant prevent the return of weight like after a banded gastric bypass and prevent postoperative bile reflux in the esophagus. The aim study is to compare primary outcome as weight loss after total wrapping of the fundus of the gastric excluded part (FundoRing) and non - wrapping (non - banded) standard method of laparoscopic one anastomosis gastric bypass and measure secondary outcome: bile reflux in the esophagus and GERD symptoms. Methods: Adult participants (n=1000) are randomly allocated to one of two groups: Experimental surgical bariatric procedure in the first (A) group: patients (n=500) undergo the laparoscopic one anastomosis gastric bypass with the total wrapping of the fundus of gastric excluded part and suture cruroplasty if present hiatal hernia (FundoRingOAGB group); Active comparator surgical bariatric procedure in the second (B) group: patients (n=500) undergo the laparoscopic one anastomosis gastric bypass and with only suture cruroplasty if present hiatal hernia (OAGB group).


Description:

One anastomosis Gastric Bypass/Mini Gastric Bypass (OAGB/MGB) is gaining popularity as a primary surgical treatment for morbid obesity. The aim study is to compare primary outcome as weight loss after total wrapping of the fundus of the gastric excluded part (FundoRing) and non - wrapping (non - banded) standard method of laparoscopic one anastomosis gastric bypass and measure secondary outcome: bile reflux in the esophagus and GERD symptoms. Methods: Adult participants (n=1000) are randomly allocated to one of two groups: Experimental surgical bariatric procedure in the first (A) group: patients (n=500) undergo the laparoscopic one anastomosis gastric bypass with the total wrapping of the fundus of gastric excluded part and suture cruroplasty if present hiatal hernia (FundoRingOAGB group); Active comparator surgical bariatric procedure in the second (B) group: patients (n=500) undergo the laparoscopic one anastomosis gastric bypass and with only suture cruroplasty if present hiatal hernia (OAGB group). All patients are then followed up 12, 24, 36 months after surgery where record the changing body mass index and and measure secondary outcome: bile reflux in the esophagus and GERD symptoms.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date May 10, 2025
Est. primary completion date April 5, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - BMI from 30 to 50 kg / m2. - The person is generally fit for anesthesia (ASA grading 1-2) and surgery. - The person commits to the need for long-term follow-up. Exclusion Criteria: - BMI less than 30 kg / m2 and more than 50 kg / m2. - Prosthetic (mesh) Hiatal herniorrhaphy or large hiatal hernia; - Esophageal shortening - Los Angeles Classification of Oesophagitis (LA grade) C or D reflux esophagitis - History of surgery on the stomach or esophagus - Less than 18 or more than 60 years of age - Not fit for bariatric surgery - Psychiatric illness - Patients unwilling or unable to provide informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
FundoRingOAGB
laparoscopic one anastomosis gastric bypass with the total wrapping of the fundus of gastric excluded part and with suture cruroplasty if present hiatal hernia
OAGB
laparoscopic one anastomosis gastric bypass with suture cruroplasty if present hiatal hernia

Locations

Country Name City State
Kazakhstan Oral Ospanov Astana

Sponsors (1)

Lead Sponsor Collaborator
The Society of Bariatric and Metabolic Surgeons of Kazakhstan

Country where clinical trial is conducted

Kazakhstan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of body mass index The measure is assessing a change of body mass index. Weight (kg) and height (cm) will be combined with the report of measurement by body mass index (BMI) kg/m2. Baseline, at 12, 24, 36 months after surgery
Secondary Postoperative bile reflux in esophagus The endoscopic finding of postoperative bile reflux in the esophagus at 12, 24, 36 months after surgery
Secondary GERD symptoms Change og GERD symptoms if present GERD or postoperative de Novo GERD symptoms (GERD-HRQL) Baseline, 12, 24, 36 months after surgery
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