Ensayos clínicos

Inclusion Criteria:

• Subject must be at least 18 years old.
• Subject is able to understand the study procedures and provide informed consent.
• Subject is willing and able to complete the entire study as specified in the protocol, including the follow-up visits.
• Subject has lung lesion that is biopsy-proven cancer (of any type) or suspicious, with confirmation at the time of the procedure.
• Lung lesion(s) are reachable/treatable per clinician opinion.
• Subject can have other location of disease if it is controlled, or there are plans for control.
• Subject has 1 or more lung nodules (not more than 10), that have a mean diameter <3 cm on axial CT scan.
• Life expectancy ≥6 months

Exclusion Criteria:

• Subject is pregnant or breast feeding.
• Subject has a significant clinical disease or condition, e.g. cardiovascular, respiratory, gastrointestinal, renal, hepatic, hematological, psychiatric or neurologic that would preclude enrollment, as determined by the primary investigator.
• Subject has another location of disease that is not controlled, and there are no plans for control.
• Subject has more than 10 lung nodules.
• If subject has acute or chronic severe renal (kidney) insufficiency (glomerular filtration rate <30 mL/min/1.73m2 they will not receive contrast with imaging.
• Subject has renal dysfunction due to the hepato-renal syndrome or in the perioperative liver transplantation period.
• > 40 BMI