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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04762849
Other study ID # UMCKazakhstan
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date April 1, 2021
Est. completion date May 1, 2024

Study information

Verified date May 2023
Source University Medical Center, Kazakhstan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Background and study aims: Currently, the gastric bypass is increasingly performed in the version of the mini gastric bypass (MGB). Another name for the procedure: one anastomosis gastric bypass (OAGB). Insufficient weight loss after bariatric surgery or weight gain after surgery is a common big problem in weight loss surgery. The use of unregulated and uncontrolled bands and rings is not always effective according to previous studies. This study compares the loss of weight after the laparoscopic banded one anastomosis gastric bypass with the use of a shape-memory ring and standard laparoscopic one anastomosis gastric bypass. Methods: Adult participants (n=100) are randomly allocated to one of two groups: Experimental surgical bariatric procedure in the first (A) group: patients (n=50) will undergo the laparoscopic banded one anastomosis gastric bypass with use of a shape-memory ring (MGB/OAGB+SMR group); Active comparator surgical bariatric procedure in the second (B) group: patients (n=50) will undergo the laparoscopic one anastomosis gastric bypass (MGB/OAGB group) without band: standard surgery. All patients are then followed up 12, 24, 36 months after surgery where record the changing body mass index.


Description:

This study compares the loss of weight after the laparoscopic banded one anastomosis gastric bypass with the use of a shape-memory ring and standard laparoscopic one anastomosis gastric bypass. Inclusion Criteria: - BMI from 30 to 50 kg / m2; - Ages Eligible for Study: 18 Years to 55 Years Outcome Measures: Change of body mass index [ Time Frame: Baseline, at 12, 24, 36 months after surgery ]


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date May 1, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: 1. Clinical diagnosis of Obesity; 2. BMI from 30 to 50 kg / m2. Exclusion Criteria: 1. Insulin-dependent diabetes; 2. BMI less than 30 kg / m2 and more than 50 kg / m2.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Laparoscopic one anastomosis gastric bypass
Laparoscopic one anastomosis gastric bypass include the creation of gastric pouch; a jejunal loop measure about 200 cm from the ligament of Treitz and anastomosed to the gastric pouch. For the creation of a gastric pouch and gastroenterostomy use a linear stapler.
Device:
A shape-memory ring for adjustable gastric banding
A shape-memory ring (SMR) use for adjustable gastric banding. SMR is placed around the gastric pouch above the gastro-entero-anastomosis.

Locations

Country Name City State
Kazakhstan University medical center Astana

Sponsors (1)

Lead Sponsor Collaborator
University Medical Center, 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
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