Determination and Validation of a Multi-analyte Assay for Lung Cancer Screening
Lung CancerThis study is part of the development and validation of a non-invasive lung screening test which aim to identify early stage lung cancer in patients at high risk for lung cancer.
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Conditions de participation
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Sexe:
ALL -
Âges admissibles:
50 to 80
Critères de participation
Inclusion Criteria - Cases:
* Current or past smokers, with at least 20 pack-years
* Subjects with either A high suspicion for lung cancer, with planned surgery to establish a definitive diagnosis within 60 days after date of blood collection OR treatment naive lung cancer patients
Exclusion Criteria - Cases:
* Known diagnosis or treatment of any previous cancer, including lung cancer, in the past 5 years, except for fully resected non-melanoma skin cancer or fully-resected carcinoma in situ of the cervix
* Current lung cancer is known to be stage III or IV by pathology.
Inclusion Criteria - Screening:
- Current or past smokers, with at least 20 pack-years, undergoing LDCT for lung cancer screening
Exclusion Criteria - Screening:
* Known diagnosis or treatment of any cancer, including lung cancer, in the past 5 years, except for fully resected non-melanoma skin cancer or fully-resected carcinoma in situ of the cervix
* Subjects whose purpose of performing LDCT is for surveillance of a lung nodule
Lieu de l'étude
University Health Network
University Health NetworkToronto, Ontario
Canada
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Vancouver General Hospital/The University of British Columbia
Vancouver General Hospital/The University of British ColumbiaVancouver, British Columbia
Canada
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McGill University Health Centre
McGill University Health CentreMontréal, Quebec
Canada
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University of Calgary
University of CalgaryCalgary, Alberta
Canada
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- Étude parrainée par
- Nucleix Ltd.
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT04968548