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Study identifier: NCT00590239 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Barrett's Esophagus Related Neoplasia (BERN) Project

Condition: Barrett's Esophagus · Neoplasms · Gastroesophageal Reflux  ·  Sponsor: Midwest Biomedical Research Foundation

PhaseN/A
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

* The use of high resolution endoscopy (HRE), narrow band imaging (NBI) and chromoendoscopy increases the detection rates of Barrett's esophagus (BE) and early neoplasia. * Endoscopic mucosal resection (EMR) will improve the accuracy for detection of dysplasia/early neoplasia. Specific Aim 1 - To create a video-atlas of non-dysplastic and dysplastic/early neoplastic lesions in patients with BE. This will be used for training purposes and to assess learning curve associated with these new technologies. Specific Aim 2 - To create a standardized classification system for the mucosal and vascular patterns observed in patients with BE. Specific Aim 3 - To determine the interobserver agreement using the video-atlas for the mucosal and vascular patterns classification agreed upon. Specific Aim 4 - To determine the endoscopic detection rate of esophageal cancer or precancerous lesions removed during endoscopy. Specific Aim 5 - To determine the pathologic and clinical outcomes of patients undergoing EMR/ablation; including morbidity, mortality and complications of the procedure. Results to date (June 2008) : this study is active and open to enrollment. Currently 26 patients have enrolled in this study at the Kansas City VA medical center. In order to participate, patients must be eligible for care at the KCVA hospital.

This description comes directly from the study's public registry record.

Talk to the study team

April Higbee, BN  ·  8168614700  ·  April.Higbee@va.gov

Always discuss trial participation with your own doctor first.

Locations (1)

Kansas city VA Medical centerKansas City, Missouri, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT00590239