Endoscopic Bariatric Therapies (EBTs): A Retrospective and Prospective Multicenter Registry

  • STATUS
    Recruiting
  • End date
    Oct 31, 2025
  • participants needed
    9999
  • sponsor
    Weill Medical College of Cornell University
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Updated on 5 August 2020
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Summary

The purpose of this registry study is to collect data through medical chart review and in patient visits on the efficacy and safety of various Endoscopic Bariatric therapies (EBTs). This is a retrospective and prospective, observational, medical chart review study for at least 6 standard of care visits up to 5 years after a subject consents for study participation.

Description

Endoscopic bariatric therapies such as intragastric balloons, space occupying EBTs, endoscopic sleeve gastroplasty (ESG), primary obesity surgery endolumenal (POSE), and small bowel interventions including gastrointestinal bypass sleeves, etc. are recommended alone or in conjunction with other weight loss treatment modules for patients who cannot or do not want to undergo conventional bariatric surgery or other therapies for obesity (with BMI 30 kg/m2) or BMI >27 with comorbidities.

This research is being done in order to find out if endoscopic bariatric therapies work as well as, or better or worse than, other currently available treatment modules to achieve weight loss.

Laboratory data, patient characteristics, imaging, histology will be collected. In certain patients - after specific consent extra blood may be collected for research purposes.

Details
Condition Weight Loss, Weight Loss, Gastroesophageal Reflux, gastroesophageal reflux disease (gerd), Obesity, Obesity, Bariatric Surgery Candidate, gastroesophageal reflux disease (gerd)
Age 18years - 89years
Treatment Endoscopic Bariatric Therapies
Clinical Study IdentifierNCT04494048
SponsorWeill Medical College of Cornell University
Last Modified on5 August 2020

Eligibility

 Yes No Not Sure

Inclusion Criteria

Any patient who is considering undergoing EBT for weight loss within 6 months, or has undergone clinically indicated EBT for weight loss within the past 6 months
Above or equal to 18 years of age

Exclusion Criteria

Any patient who has not undergone or will undergo EBT for weight loss
Below 18 years of age
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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