Clinical Trials Directory

Trials / Completed

CompletedNCT00586872

Endoscopic Mucosal Resection (EMR) in Barrett's Esophagus

Endoscopic Mucosal Resection in Barrett's Esophagus

Status
Completed
Phase
Study type
Observational
Enrollment
1,000 (actual)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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

Detailed 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.

Conditions

Timeline

Start date
2007-10-01
Primary completion
2020-06-04
Completion
2020-06-04
First posted
2008-01-07
Last updated
2022-12-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00586872. Inclusion in this directory is not an endorsement.