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NCT06339320 · ClinicalTrials.gov registry record · NA

Endoscopic Sleeve Gastroplasty (ESG) for the Treatment of Obesity

A NA study of Obesity and Endoscopic Sleeve Gastroplasty, sponsored by The Methodist Hospital Research Institute.

Recruiting
Registry status
NA
Development phase
150
Enrollment target
2
Study locations

NCT06339320 is a NA study of Obesity and Endoscopic Sleeve Gastroplasty that is actively recruiting participants, run by The Methodist Hospital Research Institute. The registered enrollment target is 150 participants, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (82% lower). The trial reports 2 study locations across 1 state.

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The verdict

NCT06339320, a NA study of Obesity and Endoscopic Sleeve Gastroplasty, is actively recruiting participants, sponsored by The Methodist Hospital Research Institute.

RECRUITING
Registry status
NA
Development phase
150 participants
Enrollment target
2
Study locations

Study 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. This procedure is FDA approved; however, Metabolic and Bariatric Surgery Accreditation and Quality Improvement Program (MBSAQIP)-Accredited centers (such as Houston Methodist Hospital) must receive approval from an Institutional Review Board (IRB) in order to perform primary procedures, such as ESG, that are not endorsed by the American Society for Metabolic and Bariatric Surgery (ASMBS).

Interventions

  • PROCEDURE Endoscopic Sleeve Gastroplasty (ESG)
  • DEVICE Apollo OverStitch endoscopic suturing device

Study Locations (2)

Texas

  • Houston Methodist Hospital - Houston
  • Houston Methodist Hospital - Sugarland - Sugar Land

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2024-02-28
Est. Completion 2033-10
Phase NA

What the Registry Record Tells You About NCT06339320

The ClinicalTrials.gov registry entry for NCT06339320 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (82% lower). The listed sponsor is The Methodist Hospital Research Institute, which has 126 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Obesity appearing as the primary indexed condition, and to 2 interventions - of which Endoscopic Sleeve Gastroplasty (ESG) is the first listed.

NCT06339320 reports 2 study locations spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT06339320 about?

NCT06339320 is a clinical study titled "Endoscopic Sleeve Gastroplasty (ESG) for the Treatment of Obesity". 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. This procedure is FDA appro...

What is the current status of trial NCT06339320?

This trial is currently recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2024-02-28. Estimated completion is 2033-10.

What conditions does trial NCT06339320 study?

This clinical trial studies the following conditions: Obesity, Endoscopic Sleeve Gastroplasty.

What interventions are being tested in trial NCT06339320?

The interventions under investigation include: Endoscopic Sleeve Gastroplasty (ESG) (PROCEDURE), Apollo OverStitch endoscopic suturing device (DEVICE).

Who is sponsoring clinical trial NCT06339320?

This trial is sponsored by The Methodist Hospital Research Institute, which has 126 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06339320 being conducted?

This trial has 2 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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