Lung Cancer Clinical Trial

Surveillance For New Lung Primaries

Summary

The primary goal of this study is to determine the prevalence of tracheobronchial carcinomas in patients with a history of squamous cell cancer of the aerodigestive tract who have been treated with a curative intent and remain disease free. Detection of pre-invasive and invasive lesions (moderate to severe dysplasia, CIS) with fluorescence bronchoscopic surveillance may help to define the natural history of these lesions and allow earlier intervention should they progress to invasive lesions.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

History squamous cell NSCLC who have undergone complete resection or definitive chemotherapy

Exclusion Criteria:

History of an aerodigestive tract carcinoma of non-squamous histology
Patients who have Stage IIIA, IIIB or IV squamous cell lung cancer that have undergone resection or chemotherapy within three years
Patients who have Stage I or II squamous cell lung cancer that have undergone resection or chemotherapy within one year
Patients who have received external beam radiation therapy for treatment of a squamous cell cancer of the lung

Study is for people with:

Lung Cancer

Estimated Enrollment:

200

Study ID:

NCT00205439

Recruitment Status:

Terminated

Sponsor:

University of Wisconsin, Madison

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There is 1 Location for this study

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University of Wisconsin Hospital and Clinics
Madison Wisconsin, 53792, United States

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Study is for people with:

Lung Cancer

Estimated Enrollment:

200

Study ID:

NCT00205439

Recruitment Status:

Terminated

Sponsor:


University of Wisconsin, Madison

How clear is this clinincal trial information?

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