About this trial
INTRODUCTION: Obesity is a critical health condition associated with high rates of morbidity and mortality. Conservative therapies such as dietary restriction, physical exercise, and pharmacological treatments have not prevented the rising incidence of obesity. Bariatric surgery, while effective, is limited to a relatively small proportion of the global obese population due to its strict indications and the risk of early and late postoperative complications. To address this gap, bariatric endoscopy therapies have emerged, offering less invasive, reversible, repeatable, and more cost-effective treatment options. The introduction of the intragastric balloon (IGB) in the 1980s marked the development of a minimally invasive, non-surgical, and safe procedure with low complication rates. OBJECTIVE: To evaluate the weight loss efficacy in overweight and Class I obese patients through the implantation of a 12-month non-adjustable intragastric balloon. METHODS: This prospective study involved overweight patients (BMI \> 27 kg/m²) undergoing intragastric balloon treatment and multidisciplinary follow-up at the Bariatric Endoscopy Clinic of the Faculty of Medicine of ABC (FMABC) over a 12-month period. EXPECTED RESULTS: Weight loss following intragastric balloon implantation and improvement in metabolic indices.
Eligibility criteria
Qualifiers
Participants with a Body Mass Index (BMI) above 27 kg/m²,
both sexes,
aged 18 years or older,
who consent to their participation by signing an Informed Consent Form and
Disqualifiers
Relative or absolute contraindications for this procedure, such as hiatal hernia (> 3 cm),
Los Angeles grade erosive esophagitis,
peptic ulcer,
prior gastric surgery,
Trial design
Treatments tested in this trial
- Non-Adjustable Intragastric Balloon
- ORBERA365