University of Florida
The aim of this multi-center study is to prospectively document the clinical utility of ESD.
Multi-center prospective data recording study. All patients will receive standard medical care and no experimental interventions will be performed. All patients scheduled to undergo ESD at the University of Florida and participating centers as medically indicated will be considered for the study. Patients in whom ESD is considered as part of their standard medical care will be offered to participate in this study. The physician performing the procedure will also discuss the study with the subjects. If the patient agrees to participate, he or she will be given the informed consent form and all…
Inclusion Criteria: * a. Age 18 years or older. * b. Scheduled to undergo ESD as part of their standard of care. Exclusion Criteria: * a. Any contraindication to performing endoscopy. * b. Participation in another research protocol that could interfere or influence the outcome measures of the present study. * c. Patient is unable/unwilling to provide informed consent.
This intervention is part of the subjects standard of care and is a method to remove the Gastrointestinal lesion.
Arctuva estimate
Verify or correct the compensation shown for this listing.