Viewing Study NCT04788199



Ignite Creation Date: 2024-05-06 @ 3:52 PM
Last Modification Date: 2024-10-26 @ 1:59 PM
Study NCT ID: NCT04788199
Status: COMPLETED
Last Update Posted: 2021-03-09
First Post: 2021-03-04

Brief Title: Novel Technique in Closure of Mesenteric Defects After Laparoscopic Roux-en-Y Gastric Bypass and Its Effect on Internal Hernia a Case-control Study
Sponsor: Mansoura University
Organization: Mansoura University

Study Overview

Official Title: Analytical Study of Internal Hernia Following Laparoscopic Roux-eny Gastric Bypass
Status: COMPLETED
Status Verified Date: 2021-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is to investigate the rate of internal hernia after laparoscopic Rox-en-Y gastric bypass when the defects are closed using cyano-acrylate glue
Detailed Description: Background Internal hernia complicated by bowel obstruction is a well-recognized complication of laparoscopic Roux-en-Y gastric bypass LRYGB The present study aims to investigate the role of cyanoacrylate glue in the prevention of internal hernia IH after LRYGB and compare it with the open technique of managing mesenteric defects by leaving the mesentery intact without closure of mesenteric defects Data from six UK hospitals have been involved in this study Operations were done under the supervision of a single senior consultant surgeon of bariatric surgery

Methods The prospectively collected data of 813 patients with morbid obesity who underwent LRYGB were retrospectively analyzed Patients were subdivided into two groups group I comprising 185 patients who had the mesenteric defects closed with cyanoacrylate glue and group II comprising 628 patients who were managed by the open technique of leaving the mesentery intact without closure of the mesenteric defects

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None