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A Study to Evaluate Glandular Atypia in Barrett’s Esophagus Determined by Volumetric Laser Endomicroscopy

Overview

About this study

The primary purpose of this study is to systematically measure the severity and extend of glandular atypia in patients with Barrett’s esophagus using volumetric laser endomicroscopy.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Patients with Barrett's Esophagus (BE) undergoing endoscopic surveillance.

Exclusion Criteria:

  • Patients with contraindications to endoscopic resection and/or volumetric laser endomicroscopy (VLE) imaging.

 

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Cadman Leggett, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

More about research at Mayo Clinic

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CLS-20482106

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