Research Site
Rio de Janeiro, 20230-130, Brazil
NCT Number: NCT07279948
A prospective, longitudinal, single-arm interventional study of lung cancer screening.
Trial opening soon.
Get Notified50 year–80 year
All sexes
Observational
Rio de Janeiro, 20230-130, Brazil
Main hypothesis: The tomographic screening for lung cancer in a population with a high prevalence of granulomatous disease could leads to an increase in the proportion of false-positive cases resulting in unnecessary medical procedures, which represents a waste of resources and a risk for patients.
Main objective: To assess whether the percentage of false-positive cases with indication of biopsy after lung cancer screening with low-dose CT in high-risk smokers in a population with a high prevalence of granulomatous disease will be within the expected range according to other studies in the literature.
As there is robust evidence of the effectiveness of screening in reducing mortality from lung cancer, we expect the project to bring benefits to patients treated for image-detected lung cancer in the project, with reduced staging and a shorter time between diagnosis and treatment. Therefore , although the focus is on the safety of screening, the project will also monitor the cancer detection rate, which is a surrogate endpoint of effectiveness.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
In order, to be eligible for the study, patients must fulfill all the following inclusion criteria:
Exclusion criteria
Time frame: Last 10 years
Tomographic screening for lung cancer in a population with a high prevalence of granulomatous disease may increase the proportion of false-positive cases, leading to unnecessary medical procedures, resource waste, and patient risk. This epidemiological scenario may also result in an increase in cases classified as benign or probably benign in screening.
Time frame: Last 10 years
Tomographic screening for lung cancer in a population with a high prevalence of granulomatous disease may increase the proportion of false-positive cases, leading to unnecessary medical procedures, resource waste, and patient risk. This epidemiological scenario may also result in an increase in cases classified as benign or probably benign in screening.
Time frame: last 10 years
Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.
Time frame: Last 10 years
Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.
Time frame: Last 10 years
Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.
Time frame: Last 10 years
Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.
Time frame: Last 10 years
Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.
Time frame: Last 10 years
Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.
Time frame: Last 10 years
Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.
Contact information is provided by the study sponsor or research team.
AstraZeneca
Industry
Acronym: LUSIP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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