Lung Cancer Clinical Trial

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Feasibility Study to Treat Lung Cancer With the Permanently Implantable LDR CivaSheet®

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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.

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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:

-

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

40

Study ID:

NCT03290534

Recruitment Status:

Recruiting

Sponsor:

CivaTech Oncology

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There is 1 Location for this study

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NYU Langone Health
New York New York, 10016, United States More Info
Mohamed El Zaeedi
Contact
Michael Zervos, MD
Principal Investigator
Benjamin Cooper, MD
Sub-Investigator

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

40

Study ID:

NCT03290534

Recruitment Status:

Recruiting

Sponsor:


CivaTech Oncology

How clear is this clinincal trial information?

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