Real-Time Optical Biopsy in Improving Lung Cancer Diagnosis in Patients Undergoing Lung Biopsy
Lesion, Lung Cancer, Diagnoses Disease

About this trial
This is an interventional diagnostic trial for Lesion focused on measuring Lesion, Lung, Cancer, Diagnosis, Optical Biopsy, Biopsy
Eligibility Criteria
Inclusion Criteria:
- Participants will be drawn from the pool of patients who have suspicious lesions identified on CT and who are already scheduled for a lung biopsy procedure with Dr. Hennemeyer or one of his colleagues
- Patients will be asked to consent to 2 to 3 extra biopsy samples to be used for this research project
Exclusion Criteria:
- Excluded from this study will be prisoners, pregnant women, patients with a contraindication for additional lung biopsies, and patients who cannot give informed consent (language barrier, cognitive impairment, etc.)
Sites / Locations
- The University of ArizonaRecruiting
Arms of the Study
Arm 1
Experimental
Diagnostic (lung biopsy)
Patients undergo extraction of up to 3 additional lung biopsies from target lesions that are at least 2-3 cm in diameter using the 19 gauge SuperCore biopsy needle or the 20 gauge Rotax needle. The extracted tissue is imaged via confocal fluorescence microscopy using a variety of fluorescent contrast agents, such as fluorescein sodium, methylene blue, indocyanine green and then undergo hematoxylin and eosin processing.