Obesity Clinical Trial - MagDI Canada Study

Status Recruiting

Clinical Trial Summary

Clinical Trial Description

The objective of the MagDI Canada study is to evaluate the performance and safety of the MagDI System in eligible participants who are indicated for a duodeno-ileal (small bowel) side-to-side anastomosis procedure for partial intestinal diversion as one example of a small bowel clinical procedure requiring a side-to-side anastomosis. The secondary objective includes initial efficacy of the duodeno-ileal diversion using the MagDI System. The partial diversion of intestinal contents from the duodenum to the ileum via side-to-side duodeno-ileostomy is intended to facilitate weight management / loss in obese adults and improve metabolic outcomes in obese adults with type 2 diabetes mellitus (T2DM). Side-to-side anastomoses are currently created by sutures, staples, and anastomotic compression devices. The most common side-to-side anastomosis technique used today is stapling, requiring cutting of the intestines and staples remain behind in the body. Linear staplers are available in different sizes (e.g., 30mm, 45mm, 50mm, 60mm). A predicate for this side-to-side duodeno-ileostomy diversion procedure is the single-anastomosis duodeno-ileostomy (SADI) procedure. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06467955
Study type	Interventional
Source	GT Metabolic Solutions, Inc.
Contact	Lisa Griffin Vincent, PhD
Phone	+1 763-200-1416
Email	clinical@gtmetabolic.com
Status	Recruiting
Phase	N/A
Start date	May 10, 2024
Completion date	August 31, 2025

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