ClinicalTrials.Veeva

Menu

Endoscopic Mucosal Resection (EMR) in Barrett's Esophagus

Mayo Clinic logo

Mayo Clinic

Status

Completed

Conditions

Early Esophageal Adenocarcinoma
Barrett's Esophagus

Study type

Observational

Funder types

Other

Identifiers

NCT00586872
07-007063 (Other Identifier)

Details and patient eligibility

About

Existing records will be reviewed to evaluate the predictors of complications including stricture formation, bleeding or perforation associated with endoscopic mucosal resection

Full description

Barrett's esophagus (BE) is a complication of gastroesophageal reflux disease in which the normal squamous lining of the esophagus is replaced by specialized columnar epithelium.1 Approximately 5%-10% of patients diagnosed with BE are thought to be at risk of developing esophageal adenocarcinoma.2 Patients with high-grade dysplasia (HGD) on biopsy are at the greatest cancer risk³. EMR is being performed clinically in our Barrett's Esophagus Unit on a regular basis during endoscopy for patients with Barrett's Esophagus and/or early esophageal adenocarcinoma. There are two predominant endoscopic mucosal resection (EMR) techniques exist using FDA approved devices - the EMR cap method using a transparent cap/snare combination and the endoscopic variceal ligation method using a band ligator/snare combination to resect tissue.

Enrollment

1,000 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Barrett's Esophagus Early Esophageal Adenocarcinoma History of Endoscopic Mucosal Resection

Exclusion criteria

  • NA

Trial design

1,000 participants in 1 patient group

1
Description:
patients with barretts esophagus and/or early esophageal adenocarcinoma who have undergone endoscopic mucosal resection

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems