About this trial
LUCIA aims to develop prediction models for the early diagnosis of lung cancer based on the identification of risk factors and deeper cellular knowledge, by recording real-world data; with risk assessment tools, non-invasive devices and omics analysis. These models will enable new clinical pathways and diagnostic workflow to be implemented to ensure early diagnosis and confirmation, including classification of lung cancer subtype.
Eligibility criteria
Qualifiers
Subjects aged between 40 and 80 years
Both genders, of which at least 37% must be women to ensure representativeness
Willingness and ability to comply with scheduled visits, laboratory tests, and other trial procedures
Written informed consent obtained prior to performing any protocol-related procedures.
Disqualifiers
Subjects under 40 years of age
Unable to be followed-up for at least 2-years or complete the study
Subjects that do not sign the informed consent
Current or prior history of lung cancer
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Biobizkaia Health Research Institute
Lead sponsor
Technion, Israel Institute of Technology
Collaborator
Centro Nacional de Análisis Genómico
Collaborator
Vicomtech
Collaborator
University of Latvia
Collaborator
Centre Hospitalier Universitaire de Liege
Collaborator
Andaluz Health Service
Collaborator
Nanose Medical Ltd.
Collaborator