Initial Feasibility Study to Treat Resectable Pancreatic Cancer With a Planar LDR Source
| Status: | Recruiting |
|---|---|
| Conditions: | Cancer, Cancer, Cancer, Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 1/17/2019 |
| Start Date: | September 6, 2017 |
| End Date: | December 31, 2020 |
| Contact: | Carra Castagnero |
| Email: | ccastagnero@tabclinical.com |
| Phone: | 9193145515 |
Initial Feasibility Study to Treat Resectable Pancreatic Cancer With the Permanently Implantable LDR CivaSheet®
This is a Phase I evaluation 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.
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.
Inclusion Criteria:
- Subject signed informed consent
- Age >/= 18 years
- Biopsy confirmed adenocarcinoma pancreatic cancer
- Patient capable of undergoing anesthesia
- Patient is a surgical candidate
- Patient selected to undergo pancreatic cancer resection
- Patient will have known or suspected close/positive surgical margin
- Confirmed diagnosis of resectable pancreatic adenocarcinoma
- Will be prescribed standard Gemcitabine 1000 mg/m2 chemotherapy cycle
Exclusion Criteria:
- Pregnant or breast feeding
- Patient has metastatic disease
- Patient has had prior radiation therapy to the region for separate cancer
- Patient has had prior chemotherapy
- Any other invasive cancer in the past 5 years, except basal cell skin
- Recurrent or previously resected tumors
- Alcoholism/Drug abuse
We found this trial at
1
site
Greenville, North Carolina
Principal Investigator: Emmanuel Zervos
Phone: 252-744-5723
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