Multi-Site Detection of Barrett's Esophagus in Patients Without Chronic GERD Symptoms

Description

The goal of this clinical trial is to develop a method to detect Barrett's esophagus in individuals with a new office based diagnostic test. Barrett's esophagus is a condition in which the flat pink lining of the swallowing tube that connects the mouth to the stomach (the esophagus) becomes damaged by acid reflux. The main question it aims to answer is: Can this approach demonstrate efficacy for screening of Barrett's esophagus? Participants will: * Participate in a questionnaire. * Undergo a capsule balloon test, called EsoCheck. * Have their EsoCheck sample sent to the laboratory for an EsoGuard test, which is used to detect Barrett's esophagus. * Participants will undergo upper endoscopy as part of standard of care.

Conditions

Barrett Esophagus, Gastroesophageal Reflux, Esophageal Adenocarcinoma

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Study Overview

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Study Details

Study overview

The goal of this clinical trial is to develop a method to detect Barrett's esophagus in individuals with a new office based diagnostic test. Barrett's esophagus is a condition in which the flat pink lining of the swallowing tube that connects the mouth to the stomach (the esophagus) becomes damaged by acid reflux. The main question it aims to answer is: Can this approach demonstrate efficacy for screening of Barrett's esophagus? Participants will: * Participate in a questionnaire. * Undergo a capsule balloon test, called EsoCheck. * Have their EsoCheck sample sent to the laboratory for an EsoGuard test, which is used to detect Barrett's esophagus. * Participants will undergo upper endoscopy as part of standard of care.

Multi-Site Detection of Barrett's Esophagus in Patients Without Chronic GERD Symptoms

Multi-Site Detection of Barrett's Esophagus in Patients Without Chronic GERD Symptoms

Condition
Barrett Esophagus
Intervention / Treatment

-

Contacts and Locations

Aurora

University of Colorado, Aurora, Colorado, United States, 80045

Baltimore

Johns Hopkins Hospital, Baltimore, Maryland, United States, 21287

Chapel Hill

University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States, 027599

Cleveland

University Hospitals Cleveland Medical Center, Cleveland, Ohio, United States, 44016

Cleveland

Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio, United States, 44195

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Adults who have not had prior EGD within past ten years, and are able to provide informed consent, and who have:
  • * No known coagulopathy, no known esophageal varices, not on chronic anticoagulation therapy, and have:
  • * No significant dysphagia or odynophagia; but who do have:
  • * Absence of GERD (absence of weekly heartburn or regurgitation, not on medications for GERD), and are:
  • * Adults \> age 50, who also have two or more added risk factors for BE from the set of: central obesity (waist size \> 35 inches for women and \> 40 inches for men), current smoker or smoking history \> 10 pack years, white race, male sex, confirmed history of BE/EAC in at least two family members, with one a first degree relative. While BE is most highly prevalent in white males, a black female over age 50 with obesity and a positive smoking history would also be at increased BE risk and would equally meet eligibility criteria.
  • * Subjects must have the ability to understand and the willingness to sign a written informed consent document.
  • * Subjects must have the ability to understand and the willingness to sign a written informed consent document.
  • * History of prior EGD procedure in past ten years
  • * Inability to provide written informed consent
  • * History of weekly of more frequent heartburn or regurgitation for five or more years
  • * On anti-coagulant drug(s) that cannot be temporarily discontinued or coagulopathy with INR \> 1.5
  • * Known history of esophageal varices or esophageal stricture
  • * Any contraindication, as deemed in Investigator's medical judgment, to undergoing the EsoCheck procedure, undergoing the EGD procedure, and/or having biopsies taken, including but not limited to due to comorbidities such as coagulopathy or a known history of esophageal diverticula, esophageal fistula and/or esophageal ulceration
  • * History of difficulty swallowing (dysphagia) or painful swallowing (odynophagia), including swallowing pills
  • * Oropharyngeal tumor
  • * History of esophageal or gastric surgery, with exception of uncomplicated surgical fundoplication procedure

Ages Eligible for Study

50 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Case Comprehensive Cancer Center,

Amitabh Chak, MD, PRINCIPAL_INVESTIGATOR, University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center

Study Record Dates

2029-09-27