Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT05574777

Endoscopic Gastric Mucosal Ablation (GMA) of Class III Obesity

Safety and Feasibility of HybridAPC for Gastric Mucosal Ablation in the Management of Patients With Class III Obesity

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Erbe Elektromedizin GmbH · Industry
Sex
All
Age
21 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study is intended to investigate safety and feasibility of a new weight loss technique called Gastric Mucosal Ablation (GMA) that does not require surgery, but can be achieved using an endoscopic procedure. Previous studies have suggested that weight loss after vertical sleeve gastrectomy (VSG) is partly due to the removal of normal stomach tissue suspected of having hormonal function. The study will investigate the minimally invasive treatment of obesity Class III participants by means of argon plasma coagulation (APC) in combination with waterjet submucosal injection using HybridAPC. As primary endpoint device or procedure related occurrence of complications according to Clavien-Dindo classification will be determined. After signing the informed consent the doctor and research team will determine if the participant meets all requirements for this study. If a participant is confirmed to be a suitable candidate additional tests will be performed prior to the first application of GMA to assess the health status of the participant prior to treatment. During the screening and baseline visit the medical history and the medications of the participant will be reviewed. After the treatments the participants will be followed for up to 6 months to assess the outcome of the GMA procedure.

Conditions

Interventions

TypeNameDescription
DEVICEHybrid Argonplasma coagulation (HAPC)Gastric mucosal ablation is an endoscopic procedure which uses argonplasma coagulation in combination with submucosal injection to achieve selective ablation to the gastric mucosa and preventing thermal damage to the muscle layer.

Timeline

Start date
2023-04-13
Primary completion
2025-08-22
Completion
2026-03-01
First posted
2022-10-12
Last updated
2026-01-22

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT05574777. Inclusion in this directory is not an endorsement.