Obese Clinical Trial
Official title:
Prospective Study Of The Procedure-less Intra-gastric Elipse Balloon: Is It Effective & Safe?
a prospective intragastric elipse balloon effect on weight loss for certain BMI. this study also proposed to assess the safety of the elipse balloon
Obesity prevalence is increasing worldwide, and Kuwait is currently considered to be the
country with the most obese population1. Accordingly, standardization of the weight loss
procedures has been made according to the Body Mass Index (BMI), keeping the more advanced
surgeries for class II obesity (BMI 35- 39.9) and above, with consideration of other factors
like, for example, obesity-related comorbidities. For those patients whom considered in the
category of overweight (BMI = 25- 29.9) & class I obesity (BMI 30- 34.9), after failure of
diet attempts, the weight loss options are limited. Of the highly requested options are the
various types of intra-gastric balloons. Conventional endoscopic gastric balloons have
proven to be safe and effective, with Excess Weight Loss (%EWL) of 25-50%2. A new
swallowable gastric balloon, named Elipse, has been launched recently in Kuwait and became
highly popular due to its unique concept of being "procedure-less".
Elipse is a weight loss device that does not require anesthesia, endoscopy, or surgery in
its "way in" or "way out". It's designed to be a swallowable capsule that is converted to a
balloon in the stomach after filling it with a PH-titrated fluid through its connected
catheter. It works by restricting the stomach and, as a result, weight loss is achieved by
decreasing the overall food quantity intake. Four months later, part of the balloon patch
side is shed-off and the fluid is expelled in the stomach in a gradual manner. Later, the
fluid and the thin paper-like wall of the balloon pass through the gastrointestinal tract
until excreted.
This prospective study aims to observe the efficacy & safety of the procedure-less
intra-gastric Elipse balloon as a tool aiding in weight loss applied to all patients in our
clinic who fulfill the criteria & underwent insertion procedure by one surgeon. In this
paper we share our experience regarding this new type of balloon, since Kuwait is one of the
first countries to start official practice with this new device and data in literature is
still lacking.
This is a prospective pilot study of 48 patients underwent Elipse balloon insertion by the
same surgeon at Faisal polyclinics in Kuwait city during six months period from July 2016 to
January 2017. After insertion, the patients were followed for a period of four months until
the expected day of excretion. Weight, BMI, & waist circumference were calculated once
pre-insertion and at 1,2, and 4 months post-insertion in the clinic. Patients were also
encouraged to send their body composition data through email using electronic scale at home
in weekly basis. All the data regarding any difficulties or adverse events during the
procedure were recorded. At the last visit, a simple questionnaire was handed to the
patients to address the commitment to peri and post procedural instructions, symptoms &
their severity encountered after insertion and excretion, overall costs spent, and patient
satisfaction. Ethical approval was obtained from the Ministry of Health in Kuwait & national
ethics committee.
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