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Clinical Trials/NCT00955019
NCT00955019
Completed
Not Applicable

Novel Method of Surveillance in Barrett's Esophagus

Mayo Clinic1 site in 1 country180 target enrollmentOctober 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Barrett Esophagus
Sponsor
Mayo Clinic
Enrollment
180
Locations
1
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

This study is being done to see how biomarkers (abnormalities in molecules of cells ) present in their Barrett's esophagus agree with results from surveillance biopsies; and to compare three different brush devices used to collect cells to see which of these 3 brush devices obtains a higher number of cells.

Detailed Description

During an endoscopy done for clinical surveillance of your Barrett's Esophagus participants are randomized to one of three brush devices by random chance like a flip of a coin. This is being done to see if one collects more cells than the others. A soft brush will be used to collect cells from the lining of the esophagus, this is known as brush cytology. With the endoscope positioned in your esophagus, samples (biopsies) of lining of the esophagus will then be taken to determine the nature of the Barrett's mucosa in the same manner as for any patient undergoing routine surveillance endoscopy for Barrett's esophagus. A part of the specimen will be used to store tissue samples that can later be used.

Registry
clinicaltrials.gov
Start Date
October 2007
End Date
September 2009
Last Updated
16 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patient age greater than 18 years of age
  • Prior histological demonstration of Barretts Esophagus that is endoscopically visible with no dysplasia
  • Low grade, high grade dysplasia or early esophageal cancer

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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