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A Study of Conforcal Fluorescent Microscopy in Barrett's Esophagus Tissue from Clinically-Indicated Endoscopic Resection

Overview

Información sobre este estudio

The purpose of this study is to test the performance characteristics of Optiscan, a handheld confocal fluorescent microscopy system, along with Ninepoint and Cellvizeo a probe based confocal microscopy system in ex-vivo Barrett’s esophagus tissue obtained from clinically-indicated, endoscopic mucosal resection (EMR) in patients scheduled for clinically indicated surveillance of Barrett's Esophagus.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:    

The study inclusion criteria include patients who are:

  1. Undergoing clinically-indicated endoscopy for Barrett’s esophagus-related neoplasia
  2. Over 18 years of age
  3. Able to provide informed consent.   

Exclusion Criteria:   

The study exclusion criteria include human subjects who are:

  1. Known to have a bleeding disorder (INR > 1.5) as this is a clinical contraindication to endoscopic mucosal resection
  2. Unable to tolerate endoscopy
  3. Women of childbearing age (menstrual period in the past three months)
  4. Severely-ill who are unsafe for routine endoscopy (i.e. on-going heart failure, difficulty breathing, and acute kidney failure)

More information

Publicaciones

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Otros temas en investigación

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CLS-20313725

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