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Initial Feasibility Study to Treat Resectable Pancreatic Cancer with the Permanently Implantable LDR CivaSheet®

Summary

The purpose of this phase I evaluation is to determine the usefulness of a new brachytherapy device that utilizes active components (Palladium-103) of standard devices in a novel configuration. This study may benefit resectable pancreatic cancer patients by reducing the radiation dose to adjacent critical structures, while giving a therapeutic dose to diseased tissue, such as at a surgical margin.

General Information

NCT#: NCT03109041
Study ID: CT005
Trial Phase: Phase I

Trial Sponsor: CivaTech Oncology
Therapies Used in This Trial: CivaSheet™

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