Actively Recruiting
Surveillance vs. Endoscopic Therapy for Barrett's Esophagus With Low-grade Dysplasia
Led by University of Colorado, Denver · Updated on 2025-11-24
680
Participants Needed
23
Research Sites
326 weeks
Total Duration
On this page
Sponsors
U
University of Colorado, Denver
Lead Sponsor
B
Baylor University
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to learn the best approach to treating patients with known or suspected Barrett's esophagus by comparing endoscopic surveillance to endoscopic eradication therapy. To diagnose and manage Barrett's esophagus and low-grade dysplasia, doctors commonly use procedures called endoscopic surveillance and endoscopic eradication therapy. Endoscopic surveillance is a type of procedure where a physician will run a tube with a light and a camera on the end of it down the patients throat and remove a small piece of tissue. The piece of tissue, called a biopsy, is about the size of the tip of a ball-point pen and is checked for abnormal cells and cancer cells. Endoscopic eradication therapy is a kind of surgery which is performed to destroy the precancerous cells at the bottom of the esophagus, so that healthy cells can grow in their place. It involves procedures to either remove precancerous tissue or burn it. These procedures can have side effects, so it is not certain whether risking those side effects is worth the benefit people get from the treatments. While both of these procedures are widely accepted approaches to managing the condition, there is not enough research to show if one is better than the other. Barrett's esophagus and low-grade dysplasia does not always worsen to high-grade dysplasia and/or cancer. In fact, it usually does not. So, if a patient's dysplasia is not worsening, doctors would rather not put patients at risk unnecessarily. On the other hand, endoscopic eradication therapy could possibly prevent the worsening of low-grade dysplasia into high-grade dysplasia or cancer (esophageal adenocarcinoma) in some patients. Researchers believe that the results of this study will help doctors choose the safest and most effective procedure for their patients with Barrett's esophagus and low-grade dysplasia. This is a multicenter study involving several academic, community and private hospitals around the United States. Up to 530 participants will be randomized. This study will also include a prospective observational cohort study of up to 150 Barrett's esophagus and low grade dysplasia patients who decline randomization in the randomized control trial but undergo endoscopic surveillance (Cohort 1) or endoscopic eradication therapy (Cohort 2), and are willing to provide longitudinal observational data.
CONDITIONS
Official Title
Surveillance vs. Endoscopic Therapy for Barrett's Esophagus With Low-grade Dysplasia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Any patient with Barrett's esophagus and low grade dysplasia who provides informed consent
- Male or female, age 18 years or older
- Endoscopic evidence of Barrett's esophagus with salmon-colored mucosa of at least 1 cm in the esophagus and biopsy showing columnar metaplasia with goblet cells
- Biopsies within the previous 12 months confirming Barrett's esophagus and low grade dysplasia
- Confirmation of low grade dysplasia by expert central pathology panel from biopsies within the previous 12 months
- Ability to tolerate proton pump inhibitor therapy and discontinue antiplatelet or anticoagulant therapy before and after endoscopic procedures according to guidelines
You will not qualify if you...
- Pregnancy
- Prior endoscopic eradication therapy for Barrett's esophagus
- History of high grade dysplasia or esophageal adenocarcinoma after endoscopy
- History of esophageal resection or esophagectomy
- Active erosive esophagitis (Los Angeles Grade B or higher) unless resolved
- Esophageal strictures preventing endoscope or treatment catheter passage unless resolved
- Esophageal varices or known portal hypertension
- Life expectancy less than 2 years as determined by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 23 locations
1
University of California, Los Angeles
Los Angeles, California, United States, 90095
Actively Recruiting
2
Kaiser Permanente Oakland Medical Center
Oakland, California, United States, 94611
Actively Recruiting
3
Kaiser Permanente
San Jose, California, United States, 95119
Actively Recruiting
4
University of Colorado
Aurora, Colorado, United States, 80045
Actively Recruiting
5
Florida Digestive Health Specialists
Sarasota, Florida, United States, 34239
Actively Recruiting
6
Northwestern Memorial Hospital
Chicago, Illinois, United States, 60611
Actively Recruiting
7
Indiana University Melvin & Bren Simon Cancer Center
Indianapolis, Indiana, United States, 46202
Actively Recruiting
8
Johns Hopkins Universtiy
Baltimore, Maryland, United States, 21205
Actively Recruiting
9
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02215
Actively Recruiting
10
University of Michigan
Ann Arbor, Michigan, United States, 48109
Actively Recruiting
11
Washington University in St. Louis
St Louis, Missouri, United States, 63110
Actively Recruiting
12
Dartmouth-Hitchcock Medical Center
Lebanon, New Hampshire, United States, 03756
Actively Recruiting
13
Long Island Jewish Medical Center
Manhasset, New York, United States, 11030
Actively Recruiting
14
Columbia Universtiy
New York, New York, United States, 10032
Actively Recruiting
15
University of Rochester Medical Center
Rochester, New York, United States, 14642
Actively Recruiting
16
University of North Carolina School of Medicine
Chapel Hill, North Carolina, United States, 27599
Actively Recruiting
17
University Hospitals Cleveland Medical Center Case Western University
Cleveland, Ohio, United States, 44106
Actively Recruiting
18
Cleveland Clinic Foundation
Cleveland, Ohio, United States, 44195
Actively Recruiting
19
University of Pennsylania, Perelman School of Medicine
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
20
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, United States, 15213
Actively Recruiting
21
Medical University of South Carolina
Charleston, South Carolina, United States, 29425
Actively Recruiting
22
Baylor University Medical Center
Dallas, Texas, United States, 75246
Actively Recruiting
23
The University of Texas MD Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
J
Jillian Welker
CONTACT
S
Sandra Boimbo
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here