Genetic risk profiles could change how we monitor Barrett's esophagus
NCT ID NCT07455422
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether sharing genetic risk information with Barrett's esophagus patients can improve their quality of life and reduce cancer worry. Researchers will collect tissue samples and use genetic analysis to create risk profiles. Half of the 266 participants will learn their risk profile, while the other half will not. The goal is to see if this approach leads to better, more cost-effective surveillance.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to more personalized and cost-effective surveillance for Barrett's esophagus patients, reducing unnecessary procedures and anxiety.
- What could go wrong
- This is an early-stage observational study, not testing a treatment. The risk model may not prove accurate enough to change practice, and results may not apply to all patients.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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AZ Delta
Roeselare, Belgium, 8800, Belgium
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Antwerp University Hospital
Edegem, Antwerpen, 2650, Belgium
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CHU LILLE - Centre Hospitalier Universitaire de Lille
Lille, 59000, France
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Ghent University Hospital (UZ Gent)
Ghent, Belgium, 9000, Belgium
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IRCCS Ospedale San Raffaele
Milan, Milano, 20132, Italy
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Karolinska University Hospital
Solna, SE-171 76, Sweden
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Rigshospitalet
Copenhagen, 2100, Denmark
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Sint-Augustinus Hospital (ZAS)
Wilrijk, Antwerpen, 2610, Belgium
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St James's Hospital
Dublin, D08 NHY1, Ireland
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University Hospital Leipzig
Leipzig, Leipzig, 04103, Germany
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Other studies related to the condition(s) this trial covers.
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