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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04627350
Other study ID # R01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 1, 2020
Est. completion date December 31, 2023

Study information

Verified date November 2020
Source Charles University, Czech Republic
Contact Lukas Lambert, M.D.
Phone +420224962232
Email lambert.lukas@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to evaluate and optimize entry criteria for the proposed programme for early detection of lung cancer in the Czech Republic. An estimated 3200 high-risk (age 55-74 years, >30 pack-years) asymptomatic individuals will undergo baseline low-dose chest CT (LDCT) and a follow-up LDCT at 1 year. Patients with poor performance status (PS) 2-4, history of malignancy in the past 10 years, chest CT in the past 1 year, bodyweight >140kg will not be included. The patients will fill out a questionnaire with basic data, including smoking history (pack-years), history of previous malignancy, CT imaging of the thorax, and will undergo spirometry. Outcomes of the study include: - optimization of entry criteria, optimization of timing of a follow-up LDCT and management of the patients, proposal of quality assurance indicators - influence of screening on the stage of lung cancer at the time of the diagnosis and life-years lost - cost-effectiveness of the screening program - evaluation of the diagnostic yield for secondary findings (pulmonary fibrosis, cardiovascular risk)


Recruitment information / eligibility

Status Recruiting
Enrollment 3200
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 55 Years to 74 Years
Eligibility Inclusion Criteria: - Age 55-74 years - Smoking: >= 30 pack-years, smoker or ex-smoker <15 years - Performance status (0-1) - can climb at least one floor without any difficulty or pause Exclusion Criteria: - Body weight above 140 kg - Malignant disease within the last 10 years (except non-melanoma skin cancer). - Chest CT less than one year ago - Clinical signs suspicious of lung cancer (weight loss, new cough, hemoptysis)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Response to pulmonary finding (nodule, mass)
Follow-up low-dose CT, PET-CT, tissue sampling (transparietal biopsy, bronchoscopy, resection), contrast-enhanced CT of the thorax

Locations

Country Name City State
Czechia General University Hospital in Prague Prague

Sponsors (2)

Lead Sponsor Collaborator
Charles University, Czech Republic General University Hospital, Prague

Country where clinical trial is conducted

Czechia, 

Outcome

Type Measure Description Time frame Safety issue
Other Number of secondary examinations The number, cost, and complications of secondary examinations generated by screening LDCT. 2023
Other Number of secondary findings The number and types of secondary findings and their clinical relevance (potentially important vs. unimportant findings) will be reported. 2023
Primary The number of cancers detected at stage I The proportion of cancers diagnosed at a resectable stage (stage I) vs. non-resectable stage (II-IV) will be compared to the stage distribution in an unscreened population 2023
Secondary The cost per diagnosis at a resectable stage The cost per diagnosis at a resectable stage will encompass the cost of low-dose CT (LDCT), follow-up LDCT, verification (PET/CT, tissue sampling, bronchoscopy). 2023
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