Actively Recruiting

Phase Not Applicable
Age: 18Years - 89Years
All Genders
NCT05753748

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

Age: 18Years - 89Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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

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