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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00205439
Other study ID # CC01506
Secondary ID 2001-431
Status Terminated
Phase
First received
Last updated
Start date December 2001
Est. completion date December 2005

Study information

Verified date July 2015
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Terminated
Enrollment 200
Est. completion date December 2005
Est. primary completion date December 2005
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 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 Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Wisconsin Hospital and Clinics Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

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