Condition: Barrett Esophagus · Barretts Esophagus With Dysplasia · Barrett's Esophagus Without Dysplasia · Sponsor: Mayo Clinic
This clinical trial evaluates the use of cytosponge, a minimally invasive collection device, for the detection of Barrett's esophagus (BE) in patients undergoing endoscopy. Non-endoscopic swallowable encapsulate sponge cell collection devices combined with markers for BE/esophageal adenocarcinoma (EAC) detection are a guideline-endorsed alternative to endoscopy for BE screening. The Oncoguard registered trademark Esophagus test (OGE) test uses esophageal cytology specimens collected with a minimally invasive, non-endoscopic, encapsulated sponge sampling device to identify BE/EAC biomarkers that indicate whether a patient should undergo diagnostic endoscopy. The OGE test is a simple and cost effective screening method that may lower barriers to widespread adoption of BE screening in at risk patients, resulting in increased and earlier detection of BE/EAC.
This description comes directly from the study's public registry record.
Clinical Trials Referral Office · 855-776-0015 · mayocliniccancerstudies@mayo.edu
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| Mayo Clinic | Scottsdale, Arizona, United States | Recruiting |
| Mayo Clinic in Florida | Jacksonville, Florida, United States | Recruiting |
| Northwestern University | Chicago, Illinois, United States | Terminated |
| Mayo Clinic in Rochester | Rochester, Minnesota, United States | Recruiting |
| Long Island Jewish Medical Center | Northwell Health | New Hyde Park, New York, United States | Completed |
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Source record: clinicaltrials.gov/study/NCT06071845