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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06076005
Other study ID # 5937
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 1, 2023
Est. completion date October 31, 2025

Study information

Verified date April 2024
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact Rocco Trisolini, MD
Phone 0630154163
Email rocco.trisolini@policlinicogemelli.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The distribution of demographic, clinical, radiological, pathological and molecular characteristics of lung cancer at the time of diagnosis, as well as preferential association between elements of those domains, have not been specifically studied in Italy. The aim of the present project is to assess, in a systematic fashion, the demographic, clinical, radiological, pathological and molecular characteristics of advanced lung cancer at the time of diagnosis in a large Italian cohort of consecutive patients referred to two tertiary referral centers.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date October 31, 2025
Est. primary completion date June 30, 2025
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age >18 years - Suspicion of lung cancer based on imaging (CT and/or PET/CT) - Indication to a biopsy for diagnosis, staging and/or molecular profiling Exclusion Criteria: - Inability or unwillingness to provide a written informed consent - ECOG performance status (>3) which makes a tissue diagnosis unfeasible - ASA 4 status - TNM Stage I-III

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Advanced lung cancer patients' group
Evaluation of the demographic, clinical, histological and molecular characteristics of advanced lung cancer at the time of Diagnosis

Locations

Country Name City State
Italy Interventional Pulmonology Division - Fondazione Policlinico Universitario A. Gemelli IRCCS Roma
Italy Istituto Nazionale Tumori Regina Elena Roma
Italy Medical Oncology Division - Fondazione Policlinico Universitario Agostino Gemelli IRCCS Roma

Sponsors (1)

Lead Sponsor Collaborator
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Distribution of histologic subtypes The investigators will assess the prevalence of histologic subtypes in patients with advanced lung cancer 24 months
Secondary Distribution of histologic subtypes according to clinical and radiological characteristics The investigators will assess the prevalence of different histologic subtypes according to clinical and imaging characteristics 24 months
Secondary Molecular profiling Prevalence of individual molecular markers in patients with advanced non-squamous non-small cell lung cancer histology 24 months
Secondary Time to diagnosis Time lag between onset of symptoms (if any) and invasive testing 24 months
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