Pancreatic Adenocarcinoma Clinical Trial
Official title:
Selective Transvenous Chemoembolization of Primary Pancreatic Tumors
Catheter directed retrograde venous infusion of gemcitabine/lipiodol into pancreatic tumors.
Overall, subjects with resectable, borderline-resectable and/or locally-advanced pancreatic
cancer are eligible to be entered into the study. Each enrolled study subject will receive a
single neoadjuvant pancreatic retrograde venous infusion (PRVI) administration of the
gemcitabine/Lipiodol® emulsion.
Complete enrollment in 12 months from date of enrollment of first study subject.
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