NCT07639684Not yet recruiting
Impact of Endoscopic Sleeve Gastroplasty (ESG) in Obese Adults With Type 2 Diabetes (T2D)
Metabolic Effects of Endoscopic Sleeve Gastroplasty in Obese Adults With Type 2 Diabetes: Evaluation of Glycemic Control, Insulin Use and Obesity Response
Source: ClinicalTrials.gov · Last updated 23 Oct 2026
Brief summary (registry, in English)
The goal of this clinical trial is to determine whether Endoscopic Sleeve Gastroplasty (ESG)-induced weight loss can improve glycemic outcomes and alter the trajectory toward insulin dependence in adults with obesity and inadequately controlled Type 2 Diabetes (T2D) despite guideline-directed therapy, including Glucagon-Like Peptide-1 Receptor Agonists (GLP-1RA)-based agents.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- First submitted
- 28 May 2026
- Start date
- Apr 2027
- Primary completion date
- Jul 2029
- Lead sponsor
- Boston Scientific Corporation
- Diseases
- Obesity, Type 2 diabetes
- NCT number
- NCT07639684
What you commit to
- Study type: Interventional
- Planned participants: 50
- From Apr 2027 to the primary completion date, Jul 2029
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study design.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Diabetes management with insulin. Prior use of insulin for gestational diabetes or short-term use (up to 1 month) in conjunction with an acute condition is acceptable.
- Noncompliance with medication regime for diabetic management
- More than one episode of clinically significant reactive or severe hypoglycemia within the prior 1 year. Reactive hypoglycemia is defined as postprandial hypoglycemia meeting Whipple's Triad; severe hypoglycemia is defined as any hypoglycemic episode requiring assistance from another person to administer carbohydrates, glucagon, or other corrective/resuscitative action
- Prior gastric surgery, including but not limited to LSG or RYGP
- Chronic systemic steroids or immunosuppressants taken at the time of enrollment or likely required during the study follow-up
- Use within the last three months prior to screening of over the counter or prescribed weight loss supplements / medications, or intent to use any weight loss medications or supplements during the study duration.
- The investigator's medical judgment that the subject is not a candidate for the ESG procedure due to findings, including but not limited to psychological and nutritional evaluation results obtained in the prior 12 months.
Other illness
- History of ketoacidosis or hyperosmolar nonketotic coma within the past 1 year
- Has a contraindication for ESG procedure with OverStitch™ or OverStitch NXT™ Endoscopic Suturing System, including but not limited to the following: large hiatal hernia, potential bleeding gastric lesions (e.g. ulcers; erosive gastritis, varices, or vascular malformation), coagulopathy and antiplatelet/anticoagulant therapy that cannot be correct
- Any known conditions that impact weight loss or glycemic management
Lab values
- CKD stage 3+, defined as eGFR \< 60 mL/min
- Persistent anemia, defined as hemoglobin \< 10 g/dL
Other
- Excessive alcohol consumption, defined as meeting or exceeding sex-based heavy drinking limits
- Current pregnancy confirmed by site standard of care or planned pregnancy or breastfeeding for a year following the ESG procedure.
- Vulnerable subject.
- Current or planned participation in another clinical study.
Who the study is looking for
- Willing and able to provide written informed consent to participate in the study
- Age ≥ 22 years
- BMI 30 - 50 kg/m2
- HbA1c 7.5 - 10.5%
- Type 2 Diabetes treated with incretin-based medication (aka GLP-1RA agonist or GLP-1RA/GIP dual agonist) at a stable, maximal tolerated dose for a minimum of 6 months +/- any other oral glucose lowering medications AND intention to initiate insulin therapy for glycemic management
- Stable weight (\< 5% TBW) within the 3 months prior to screening
- Meets the indications for ESG procedure with OverStitch™ or OverStitch NXT™ Endoscopic Suturing System, excluding the following but not limited to the following: large hiatal hernia, potential bleeding gastric lesions (e.g. ulcers; erosive gastritis; varices; or vascular malformation), coagulopathy and antiplatelet/anticoagulant therapy that cannot be corrected
- Declines or is ineligible for metabolic bariatric surgery
- Agrees to abstain from taking any weight loss treatments or supplements that are not part of the lifestyle modification program for a year following the ESG procedure
- Willing and able to comply with the study procedure with standard of care lifestyle modification program and visit schedule.
Age in the registry: 22 years to - · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.