Endoscopic Bariatric Therapies (EBTs): A Retrospective and Prospective Multicenter Registry
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- STATUS
- Recruiting
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- End date
- Oct 31, 2025
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- participants needed
- 9999
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- sponsor
- Weill Medical College of Cornell University
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 Identifier | NCT04494048 |
| Sponsor | Weill Medical College of Cornell University |
| Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf 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.
Learn moreComplete 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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