Last updated: December 5, 2023
Sponsor: True You Weight Loss
Overall Status: Active - Not Recruiting
Phase
N/A
Condition
Obesity
Weight Loss
Diabetes Prevention
Treatment
Apollo ESG
Fundic Mucosal Ablation with ERBE HybridAPC
Fundic Ablation in Combination with Endoscopic Sleeve Gastroplasty
Clinical Study ID
NCT05992103
PS-002
Ages 21-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Subjects aged 21-65
- Body mass Index (BMI) ≥30 kilograms per square meter (kg/m²), or ≤50 kg/m²
- History of at least one unsuccessful dietary effort to lose body weight
- Willing and able to participate in the study procedures
- Understand and voluntarily sign the informed consent
- Approved ESG candidate at True You Weight Loss
- Access to internet
- Reliable transportation to and from Cary, North Carolina surrounding area
Exclusion
Exclusion Criteria:
- Younger than 21 years of age
- Older than 65 years of age
- Patients on any medications or supplements including those that may influencecholecystokinin (CCK), glucose, growth hormone, insulin and/or somatostatin levels
- Milk and/or soy allergies
- History of any stomach manipulation (including repair of hiatal hernia)
- History of disordered eating
- Patients who do not give their consent to the enrollment in the study or areincompetent, unconscious or unable to express their consent for any reason
- Hemoglobin A1c > 7.0 or any patient with symptoms suggestive of gastroparesis or aformal diagnosis of gastroparesis
- Patients taking the following medications known to impair gastric accommodation:buspirone, mirtazapine
- Patients taking the following medications known to accelerate or impair gastricemptying: Reglan (metoclopramide), Zelnorm (tegaserod), Motegrity (prucalopride),erythromycin, Motilium (domperidone), opiates, anticholinergic agents
- Patients who are pregnant or who plan to become pregnant during study duration
- Use of non-steroidal anti-inflammatory medications without the ability to stop theseduring study duration
- Patients on chronic anticoagulation
- History of functional gastrointestinal disorder, including functional dyspepsia,irritable bowel syndrome, or other syndromes known to affect gastric sensorimotorfunction.
- Concurrent use of weight loss medications.
Study Design
Total Participants: 10
Treatment Group(s): 3
Primary Treatment: Apollo ESG
Phase:
Study Start date:
September 14, 2023
Estimated Completion Date:
May 15, 2025
Study Description
Connect with a study center
True You Weight Loss
Cary, North Carolina 27513
United StatesSite Not Available
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