- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03316053
Cell Marker Predictors in Barrett's Esophagus
January 5, 2026 updated by: The Guthrie Clinic
The purpose of this study is to analyze biopsied tissue samples for changes in cells and genes involved in Barrett's Esophagus.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
Patients with a history of Barrett's esophagus who are scheduled for a routine endoscopy will have an additional biopsy taken for genetic testing.
Study Type
Observational
Enrollment (Estimated)
25
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pennsylvania
-
Sayre, Pennsylvania, United States, 18840
- The Guthrie Clinic
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients with a history of Barrett's esophagus
Description
Inclusion Criteria:
- History of Barrett's esophagus; scheduled for routine upper endoscopy
Exclusion Criteria:
- Under 18 years of age
- Unable to consent on own behalf
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Tissue Sample for genetic testing
Biopsy sample
|
Tissue sample to be obtained during routine endoscopy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cell Markers
Time Frame: through study completion, an average of 1 year
|
Identify genes involved in Barrett's Esophagus
|
through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Michael Georgetson, MD, The Guthrie Clinic
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 15, 2017
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2027
Study Registration Dates
First Submitted
October 16, 2017
First Submitted That Met QC Criteria
October 18, 2017
First Posted (Actual)
October 20, 2017
Study Record Updates
Last Update Posted (Estimated)
January 7, 2026
Last Update Submitted That Met QC Criteria
January 5, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Neoplasms
- Digestive System Diseases
- Gastrointestinal Diseases
- Esophageal Diseases
- Precancerous Conditions
- Barrett Esophagus
- Investigative Techniques
- Clinical Laboratory Techniques
- Diagnostic Techniques and Procedures
- Diagnosis
- Health Services
- Health Care Facilities Workforce and Services
- Preventive Health Services
- Immunologic Techniques
- Genetic Techniques
- Genetic Services
- Diagnostic Services
- Immunologic Tests
- Genetic Testing
- Histocompatibility Testing
Other Study ID Numbers
- 1708-43
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.