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NCT05145205 Clinical Trial

Laparoscopic Sleeve Gastrectomy vs Laparoscopic Roux-en-Y Gastric Bypass

Laparoscopic Surgery Clinical Trial

Official title:
Effect of Laparoscopic Sleeve Gastrectomy vs Laparoscopic Roux-en-Y Gastric Bypass on Weight Loss in Patients With Morbid Obesity

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05145205
Other study ID # AUH210021
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2020
Est. completion date December 31, 2020

Study information
Verified date November 2021
Source Al-Azhar University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a retrospective work on 200 morbid obese patients randomized and categorized into 2 groups according to the treatment method: the laparoscopic sleeve gastrectomy (LSG) and LRYGB groups, within the period from 2014 to 2019 and matched weight dissipation, complications, life quality, and negative events

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - All patients of (Body Mass Index) more than 40, with at least 1 comorbidity Exclusion Criteria: - All patients of (Body Mass Index) less than 40, - No comorbidities - Patients who refused the surgical procedures.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Sleeve gastrectomy
Bougie was applied over the lower curvature to adjust the gastric tube then longitudinal amputation of the stomach was performed for about 4 to 6 cm per pecker of the pylorus to the corner of His. No supportive materials were used, and over-suturing of the basic line performed only over the points of bleeding. All resected specimens were sent to histopathology laboratory for examination.
• Laparoscopic Roux-en-Y gastric bypass
An antecolic and antegastric RYGB become executed with a 150 cm alimentary limb with both a linearly or circularly kink (25 mm) gastrojejunostomy in step with the desire of the surgeon. A 50-cm-lengthy biliopancreati

Locations
Country Name City State
Egypt Azhar faculty of medicine Cairo

Sponsors (1)
Lead Sponsor Collaborator
Al-Azhar University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary weight dissipation decrease the body mass index by 1 or more 12 months
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