Building a multiomic database using advanced imaging techniques

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to create a large-scale multiomic database by enrolling adult patients undergoing advanced imaging studies, specifically using Photon Counting CT and 3T MRI. The study will collect imaging raw data, clinical, demographic, and laboratory test results, as well as genetic testing information when available. Patients will be followed annually to update their clinical and imaging data, allowing for a comprehensive analysis of the latent information derived from these advanced imaging modalities. The goal is to explore the potential of these 'opportunist features' in enhancing patient characterization and improving screening and prevention strategies.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adult subjects (\>18 y.o.) submitted to Computed Tomography (CT) using Photon Counting CT scanner (Neaotom Alpha, Siemens) and Magnetic Resonance (MRI) exams acquired with 3T scanner (MR 7700, Philips) for examination required for clinical practice or for clinical trials at the IRCCS San Raffaele Hospital who signe an Informed Consent authorizing data collection.

Exclusion Criteria:

* Absent informed consent signed

Where it's running

• IRCCS San Raffaele
  Milan, Italy Recruiting

Study contacts

• Study coordinator: Antonio Esposito
• Email: esposito.antonio@hsr.it
• Phone: 0226436102

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.