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Endoscopic Sleeve Gastroplasty (ESG) for the Treatment of Obesity

NCT06339320

This study is recruiting at 2 US sites in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

The purpose of this study is to evaluate endoscopic sleeve gastroplasty (ESG) for the treatment of obesity. The ESG procedure is an U.S. Food and Drug Administration (FDA) approved procedure for the treatment of obesity - patients with a body mass index (BMI) 30-50 kg/m2.

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

Conditions studied

  • Endoscopic Sleeve Gastroplasty
  • Obesity

Eligibility basics and study details

Study type
Interventional
Phase
Not applicable
Ages
18 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
The Methodist Hospital Research Institute
Last updated on ClinicalTrials.gov
April 1, 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

Texas · 2

  • Houston Methodist Hospital · Houston, TX
  • Houston Methodist Hospital - Sugarland · Sugar Land, TX

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