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A Prospective Study on the Interobserver Agreement of Endoscopic Barrett's Esophagus


N/A
18 Years
80 Years
Not Enrolling
Both
Barrett's Esophagus, GERD

Thank you

Trial Information

A Prospective Study on the Interobserver Agreement of Endoscopic Barrett's Esophagus


Inclusion Criteria:



- History of (h/o) GERD

- Upper GI symptoms such as acid taste in mouth, dysphagia, dyspepsia

- Screening or surveillance exam for BE

Exclusion Criteria:

- Unable to consent

- History of esophageal varices

Type of Study:

Observational

Study Design:

Observational Model: Case-Only, Time Perspective: Prospective

Outcome Measure:

The primary outcome will be the interobserver variability in the presence of columnar epithelium as well as the measured lengths.

Outcome Time Frame:

one endoscopy visit

Safety Issue:

No

Principal Investigator

Glenn M Eisen, MD, MPH

Investigator Role:

Principal Investigator

Investigator Affiliation:

Oregon Health and Science University

Authority:

United States: Institutional Review Board

Study ID:

IRB00003558

NCT ID:

NCT00591461

Start Date:

December 2007

Completion Date:

December 2009

Related Keywords:

  • Barrett's Esophagus
  • GERD
  • Barrett's Esophagus
  • Upper Endoscopy
  • Esophageal biopsies
  • Accuracy
  • Interobserver Agreement
  • Barrett Esophagus

Name

Location

OHSUPortland, Oregon  97239
PVAMCPortland, Oregon  97239