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(for at least one location)
Scottsdale/Phoenix, AZ, Austin, MN, Eau Claire, WI, Jacksonville, FL, La Crosse, WI, Mankato, MN, Rochester, MN
Describes the nature of a clinical study. Types include:
This study will evaluate if the sponge capsule device can accurately detect the presence of Barrett's Esophagus and prevalent dysplasia/adenocarcinoma detection, in a screening population, with and without chronic gastroesophageal reflux disease.
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Open for enrollment
Closed for enrollment
Rochester, MN, Scottsdale/Phoenix, AZ
The purpose of this study is to compare the effectiveness of two approaches for the management of Barrett's Esophagus (BE) and Low-grade Dysplasia (LGD), endoscopic surveillance and endoscopic eradication therapy (EET), using accepted clinical endpoints of neoplastic progression [high-grade dysplasia (HGD)/mucosal esophageal adenocarcinoma (EAC)/invasive EAC] as determined by a blinded central committee.
Scottsdale/Phoenix, AZ
The purpose of this study is to elicit patients’ perceptions around their experience with Barrett's Esophagus (BE) and characterize barriers and potential solutions to care resulting in delayed surveillance or loss to follow-up using a mixed-methods approach.