Evaluation of Endoscopic Sleeve Gastroplasty (ESG) as an Alternative Weight Loss Strategy for Patients With Obesity Discontinuing GLP-1 Receptor Agonists Due to Intolerance or Ineffectiveness: A Retrospective Study

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Behavioral, Device
Study Type: Observational
SUMMARY

This study is designed to compare weight loss outcomes and safety of ESG versus lifestyle modification in patients with obesity who discontinued GLP-1 therapy due to intolerance or suboptimal weight loss.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adults (≥ 18 years)

• BMI ≥30 kg/m² and ≤ 50 kg/m2

• Discontinued GLP-1 therapy for weight loss (semaglutide and tirzepatide only) for intolerance or suboptimal weight loss (\<5% TBWL after 3 months at maximally tolerated dose)

• Initiation of weight loss management between August 2021 and September 2024

• Completed 1-year follow-up for weight loss management (ESG and lifestyle modification or lifestyle modification alone) following initiation of weight loss treatment

• Completed at least two interim visits for weight loss management from 1, 3, 6, through 9 months following initiation of weight loss treatment

Locations
United States
Florida
Bariendo
RECRUITING
Miami
Massachusetts
Brigham & Women's Hospital
NOT_YET_RECRUITING
Boston
West Virginia
West Virginia University
NOT_YET_RECRUITING
Morgantown
Contact Information
Primary
Katherine Stroud
katherine.stroud@bsci.com
617-233-5845
Backup
Pooja Goswamy
pooja.goswamy@bsci.com
508-683-4335
Time Frame
Start Date: 2025-12
Estimated Completion Date: 2026-06
Participants
Target number of participants: 150
Treatments
ESG Recipients
After discontinuing GLP-1 medication, this group elected to have an ESG procedure as a weight loss treatment.
Lifestyle Modification
After discontinuing GLP-1 medication, this group elected to participate in a structured lifestyle modification program.
Related Therapeutic Areas
Sponsors
Leads: Boston Scientific Corporation

This content was sourced from clinicaltrials.gov