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NCT Number: NCT07279948

Lung Cancer Screening Implementation Project in the Brazilian Public Health Care System (LUSIP)

A prospective, longitudinal, single-arm interventional study of lung cancer screening.

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Key information

Age range

50 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Research Site

Rio de Janeiro, 20230-130, Brazil

About this study

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.

Who can participate

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:

  • Age between ≥50 and ≤80 years.
  • Be a current smoker or have quit 15 years ago or less.
  • Have participated or are currently participating in smoking cessation program.
  • Lifetime smoking exposure equal to or greater than 20 pack-year.
  • Provided signed informed consent (ICF)

Exclusion criteria

  • In order, to be exclude for the study, patients must at least one of the following exclusion criteria:
  • Contraindications to the screening examination: (claustrophobic or weighing more than 130 kgs).
  • Inability to climb 3 stair steps non-stop (36 steps).
  • Disabling dyspnea
  • Symptomatic (with signs and symptoms suspicious of breast cancer lung, namely):
  • pleuritic chest pain
  • rapidly progressive dyspnea of recent onset
  • hemoptysis
  • unexplained hoarseness, lasting more than 1 month.
  • bone pain
  • supraclavicular lymphadenopathy or cervical lymphadenopathy persistent
  • unexplained weight loss of 5% or more of weight in less than 6 months
  • Previous history of malignant neoplasm (excluding non-melanoma skin cancer) diagnosed less than 10 years before the date of the interview;
  • Patients with diagnostic of severe psychiatric disease
  • Immunosuppressed by illness or drugs.
  • Subjected to anterior lung resection even when determined due to an etiology other than malignant neoplasia.
  • Person with a serious terminal illness that contraindicates curative lung surgery.

Treatment and study plan

Primary outcomes

  1. • Proportion of negative cases on screening according to the Lung-RADS classification.

    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.

  2. • Proportion of false-positives.

    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.

Secondary outcomes

  1. • Cancer detection rate.

    Time frame: last 10 years

    Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.

  2. • Willingness to be screened (ie, proportion of eligible patients actually signing up for the study)

    Time frame: Last 10 years

    Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.

  3. • Percentage of adherence to screening - calculated by dividing the number of individuals screened with LDCT (numerator) by the number of eligible individuals invited to screen (denominator).

    Time frame: Last 10 years

    Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.

  4. • Percentage of adherence to follow-up.

    Time frame: Last 10 years

    Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.

  5. • Prevalence of granulomatous disease in screening positive cases

    Time frame: Last 10 years

    Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.

  6. • Prevalence of incidental findings.

    Time frame: Last 10 years

    Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.

  7. • Prevalence of clinically relevant incidental findings that required follow-up.

    Time frame: Last 10 years

    Not Applicable (N/A). The findings of each outcome will be compared with results published in the scientific literature.

Study contacts

Contact information is provided by the study sponsor or research team.

AstraZeneca Clinical Study Information Center

CONTACT

[email protected]

1-877-240-9479

Sponsors and collaborators

Lead sponsor

AstraZeneca

Industry

Registry information

Acronym: LUSIP

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Dec 12, 2025
Registry last updated
Jun 25, 2026

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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