Ultralong-segment Barrett's Esophagus: Towards a Capsule-sponge Surveillance Strategy

Recruiting N/A Interventional Study
Barrett Esophagus
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
137 (estimated)
Sponsor
Erasmus Medical Center · Other
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About This Trial

The purpose of this study is to evaluate the Endosign capsule sponge test as a novel surveillance method in patients with an ultralong-segment Barrett's esophagus.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Any participant 18 years and above, with ultralong-segment Barrett's esophagus and clinically fit for an endoscopy * Ability to provide informed consent Exclusion Criteria: * Individuals with a diagnosis of an oro-pharynx, esophageal or gastro-esophageal tumor (T2 staging an…
Contacts

Anne-Elise C de Groen, MSc

003110 703 16 93

a.degroen@erasmusmc.nl

CONTACT

Judith Honing, MSc, PhD

003110 703 16 93

j.honing@erasmusmc.nl

CONTACT