Clinical Trial VICCTHO0373
Title
Identification and Validation of Molecular Markers in Lung Cancer (SPORE)
Principal Investigator(s)
Details
- Protocol No. VICCTHO0373
- Open Date: 05/03/2001
- Staging: Pilot
- Age Group: Adults
- Scope: Local
- Objective:
- Disease Sites: Lung
- Therapies: None Specified
- Drugs: None Specified
- Participating Institutions: Vanderbilt University; Veterans Administration
- National Clinical Trial ID: NCT00899028
- Secondary Protocol No: VICCTHO0373
Description
None Provided.
Eligibility
| Ages Eligible for Study: | 18 Years and older |
|---|---|
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Accepts Healthy Volunteers |
Criteria
DISEASE CHARACTERISTICS:
• Meets 1 of the following criteria:
• Known or previously diagnosed lung cancer
• Suspected lung cancer, including the following:
• Completely resected stage I lung cancer (with no evidence of metastatic disease) for which patient is at risk for developing secondary disease
• Suspected of having lung cancer due to clinical symptoms, such as positive sputum cytology, hemoptysis, unresolved pneumonia, persistent cough, and positive x-ray
• Healthy volunteer
PATIENT CHARACTERISTICS:
• WBC ≥ 2,000/mm³ but ≤ 20,000/mm³
• Platelet count ≥ 50,000/mm³
• Not pregnant
• No uncontrolled hypertension (i.e., systolic blood pressure > 200 mm Hg, diastolic blood pressure > 120 mm Hg)
• No unstable angina
• No known bleeding disorder
• No other contraindications for white light bronchoscopic examination
• No other contraindications for fluorescence examination
PRIOR CONCURRENT THERAPY:
• More than 3 months since prior fluorescent photosensitizing agents (hematoporphyrin derivatives)
• More than 3 months since prior and no concurrent chemopreventative drugs (e.g., tretinoin)
• More than 6 months since prior ionizing radiation treatment to the chest
• More than 6 months since prior systemic cytotoxic chemotherapy
• No concurrent anticoagulant therapy
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