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REvision of VSG with Ablation of the Mucosa Procedure

NCT06671119

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

The purpose of this study is to evaluate the feasibility, safety, and tolerability of endoscopic selective gastric mucosal ablation (GMA) using argon plasma coagulation after sleeve gastrectomy. In this study, GMA will be performed on patients who have experienced weight regain following an initial successful response to sleeve gastrectomy.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Obesity and Obesity-related Medical Conditions
  • Obesity and Overweight
  • Obesity Prevention
  • Obesity Recidivism

Eligibility basics and study details

Study type
Interventional
Phase
Not applicable
Ages
22 to 60 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Dr. Christopher McGowan
Last updated on ClinicalTrials.gov
November 5, 2024

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

North Carolina · 1

  • True You Weight Loss · Cary, NC

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.