Obesity Clinical Trial
— AW2Official title:
Single-Stage Gastric Fundus Ablation and Endoscopic Sleeve Gastroplasty for Weight Loss
Verified date | December 2023 |
Source | True You Weight Loss |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this research is to investigate the combined effects of fundic ablation (FA) and endoscopic sleeve gastroplasty on circulating plasma ghrelin, satiation, and total body weight loss, as well as the incidence of adverse events. This procedure will be carried out with the HybridAPC (ERBE Elektromedizin GmbH, Tübingen, Germany). The HybridAPC instrument creates an electric current to deliver a safe amount of thermal injury to a portion of the stomach known as the gastric fundus. This thermal injury will target a hormone called ghrelin which is the only known hormone linked to increasing appetite, calorie intake, and weight gain. This procedure is designed to target the bodily effects of appetite control and gastric sensory and motor functions which cause the feeling of fullness and satiation. When fundic mucosal ablation is paired with endoscopic sleeve gastroplasty (ESG), this combined investigational approach may lead to decreased fasting ghrelin levels, improved satiation, and greater total body weight loss than traditional ESG. This study will help determine if the combined impact of FA with ESG within the same endoscopic session should be made available to patients as part of a comprehensive weight loss strategy.
Status | Active, not recruiting |
Enrollment | 10 |
Est. completion date | May 15, 2025 |
Est. primary completion date | April 14, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 21 Years to 65 Years |
Eligibility | Inclusion Criteria: 1. Subjects aged 21-65 2. Body mass Index (BMI) =30 kilograms per square meter (kg/m²), or =50 kg/m² 3. History of at least one unsuccessful dietary effort to lose body weight 4. Willing and able to participate in the study procedures 5. Understand and voluntarily sign the informed consent 6. Approved ESG candidate at True You Weight Loss 7. Access to internet 8. Reliable transportation to and from Cary, North Carolina surrounding area Exclusion Criteria: 1. Younger than 21 years of age 2. Older than 65 years of age 3. Patients on any medications or supplements including those that may influence cholecystokinin (CCK), glucose, growth hormone, insulin and/or somatostatin levels 4. Milk and/or soy allergies 5. History of any stomach manipulation (including repair of hiatal hernia) 6. History of disordered eating 7. Patients who do not give their consent to the enrollment in the study or are incompetent, unconscious or unable to express their consent for any reason 8. Hemoglobin A1c > 7.0 or any patient with symptoms suggestive of gastroparesis or a formal diagnosis of gastroparesis 9. Patients taking the following medications known to impair gastric accommodation: buspirone, mirtazapine 10. Patients taking the following medications known to accelerate or impair gastric emptying: Reglan (metoclopramide), Zelnorm (tegaserod), Motegrity (prucalopride), erythromycin, Motilium (domperidone), opiates, anticholinergic agents 11. Patients who are pregnant or who plan to become pregnant during study duration 12. Use of non-steroidal anti-inflammatory medications without the ability to stop these during study duration 13. Patients on chronic anticoagulation 14. History of functional gastrointestinal disorder, including functional dyspepsia, irritable bowel syndrome, or other syndromes known to affect gastric sensorimotor function. 15. Concurrent use of weight loss medications. |
Country | Name | City | State |
---|---|---|---|
United States | True You Weight Loss | Cary | North Carolina |
Lead Sponsor | Collaborator |
---|---|
True You Weight Loss |
United States,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of Safety Complications | Occurrence of Grade III - V complications according to the Clavien-Dindo classification | Week 1, Month 1, Month 2, Month 3, Month 4, Month 6, Month 7, Month 8, Month 9, Month 10, Month 11, Month 12 | |
Primary | Rate of Adverse Events | Occurrence of Adverse Events and Serious Adverse Events | Week 1, Month 1, Month 2, Month 3, Month 4, Month 6, Month 7, Month 8, Month 9, Month 10, Month 11, Month 12 | |
Secondary | Percent Change in Total Body Weight Loss (TBWL) from Baseline | Measure percent change in total body weight over time following FA-ESG. TBWL = pre-op weight - post op body weight. % TBWL is the fraction of body weight expressed in percentage term | Week 1, Month 1, Month 2, Month 3, Month 4, Month 6, Month 7, Month 8, Month 9, Month 10, Month 11, Month 12 |
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