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NOT YET RECRUITING
NCT07455422
NA

A Study of Barrett's Esophagus Patients: Optimization of a Risk Model to Better Predict the Development of Cancer Recurrence and the Effect of Risk Profile Disclosure on Patient Quality of Life and Fear of Cancer

Sponsor: University Hospital, Antwerp

View on ClinicalTrials.gov

Summary

The goal of the study is: * The collection of various tissue samples (blood, biopsies and "esophageal brushes") and their analysis. * To test a risk model based on genetic analyses (DNA-FISH and so-called single cell sequencing) on esophageal tissue samples. * Evaluating the quality of life of Barrett's Esophagus patients and the degree of fear of getting cancer. Patients with a Barrett's Esophagus can participate in the study if they are minimally 18 years old, are capable of giving informed consent (fully understanding what the study entails before giving consent to participate), have Barrett Esophagus and are referred to one of the participating centers due to suspicion of early esophageal cancer, for which the participant will be evaluated by endoscopic imaging and biopsy. Study procedures: An intake consultation will be planned, wherein the eligibility criteria will be assessed, and participant characteristics will be collected. A routine gastroscopy will be planned twice during which several minimally-invasive interventions will be performed: drawing a blood sample, brush cytology during the endoscopy (a brush is used to obtain cells from the surface of the esophagus) and obtaining biopsy samples (small pieces of tissue). Each participant will need to undergo all the interventions. Patients will have to complete questionnaires at several time points to assess their quality of life (EQ-5D-DL questionnaire) and fear of cancer recurrence (Cancer Worry Scale). This study is a randomized trial, meaning the study participants will be divided into two groups by the computer. One group will be informed of their risk profile, established based on the genetic analyses. The other group will not be informed of their risk profile. All patients will be followed-up in a more intensive surveillance schedule compared to the standard of care, for study purposes.

Official title: A Randomized Controlled Trial Using Endoscopic Brush Cytology and Single Cell Clonal Dynamics of Early ESOPHAGEAL ADENOCARCINOMA for Assessing Effects on Quality of Life, Cancer Worry and Defining Cost-Effective Surveillance Strategies

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

266

Start Date

2026-06-01

Completion Date

2030-12-31

Last Updated

2026-03-06

Healthy Volunteers

No

Interventions

OTHER

Risk profile disclosure

Participants in the intervention arm will be informed by the investigator on their genetic risk profile.

Locations (10)

Antwerp University Hospital

Edegem, Antwerpen, Belgium

Sint-Augustinus Hospital (ZAS)

Wilrijk, Antwerpen, Belgium

Ghent University Hospital (UZ Gent)

Ghent, Belgium, Belgium

AZ Delta

Roeselare, Belgium, Belgium

Rigshospitalet

Copenhagen, Denmark

CHU LILLE - Centre Hospitalier Universitaire de Lille

Lille, France

University Hospital Leipzig

Leipzig, Leipzig, Germany

St James's Hospital

Dublin, Ireland

IRCCS Ospedale San Raffaele

Milan, Milano, Italy

Karolinska University Hospital

Solna, Sweden