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Prospective Study to Compare the Efficacy of E.G.Scan to Detect Barrett's Esophagus Compared With Standard Endoscopy

Barrett's Esophagus Clinical Trial

Official title:
Prospective Study to Compare the Efficacy of E.G.Scan to Detect Barrett's Esophagus Compared With Standard Endoscopy

Clinical Trial Summary

Will EG Scan (transnasal endoscopy) determine presence of Barrett's Esophagus, esophagitis and hiatal hernia as well as standard sedated endoscopy.

Clinical Trial Description

To evaluate the sensitivity and specificity of E.G.Scan (transnasal endoscopy) in diagnosing Barrett's Esophagus (using standardized endoscopic criteria) compared with the gold standard white light sedated endoscopy.

To look at the sensitivity and specificity of E.G.Scan (transnsasal endoscopy) in diagnosing short segment Barrett's Esophagus, esophagitis and hiatus hernia. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02066233
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase N/A
Start date March 2014
Completion date March 2016
View Details
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