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[Charlotte] => https://www.survivornet.com/charlotte/
[Cleveland] => https://www.survivornet.com/cleveland/
[Columbus] => https://www.survivornet.com/columbus/
[Dallas / Ft. Worth] => https://www.survivornet.com/dallas-ftworth/
[Denver] => https://www.survivornet.com/denver/
[Detroit] => https://www.survivornet.com/detroit/
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Feasibility Study to Treat Lung Cancer With the Permanently Implantable LDR CivaSheet® Summary This is a feasibility study to determine the usefulness of a brachytherapy device that utilizes active components (palladium-103) of standard devices in a novel configuration, which may benefit lung cancer patients by reducing the radiation dose to critical structures, such as the heart wall, while giving a therapeutic dose to diseased tissue, such as at a surgical margin.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Subject signed inform consent Suspected or proven non-small cell lung cancer (NSCLC) in the upper lobes of the left or right lung Pre-operative criteria Lung nodule suspicious for NSCLC Mass ≤ 7 cm in maximum diameter by CT scan of the chest and upper abdomen Clinical stage I or Clinical stage II Not pregnant or nursing Negative pregnancy test in premenopausal women Fertile patients must use effective contraception More than 5 years since prior invasive malignancy unless non melanoma skin cancer or in-situ cancer Exclusion Criteria: -
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There is 1 Location for this study
NYU Langone Health New York New York, 10016, United States
More Info How clear is this clinincal trial information?
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