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Recruiting Observational

Non-Invasive Diagnosis and Monitoring of Cardiac Masses by Liquid Biopsy

NCT07235865 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-07-25
Last updated
2026-04-15

Condition(s) studied

Cardiac Masses

Investigational drug(s) / intervention(s)

NGS-guided regimen: Regimen A

NGS-guided regimen: Regimen A: Liquid biopsy, consisting of a venous blood sample, will be collected during routine venipuncture

Study summary

This is a nonprofit, observational, prospective and retrospective,multicenter study in a population of young and adult patients ≥12 years with a diagnosis of a cardiac mass. The study will include both patients with masses of unknown pathological diagnosis and patients with a known histology of benign or malignant tumors. We predict a case-control allocation ratio of 1:1 between cardiac malignant tumors and benign lesions. Peripheral blood will be collected at participating centers during routine venipuncture,processed and then shipped for liquid biopsy ctDNA NGS analyses. If available, in malignant cases, matched tumor tissue samples collected as per clinical practice solid biopsies or surgery will be used for analyses. Longitudinal tracking through serial blood draws could be performed in selected cases of patients with cardiac malignancies who receive cancer treatment

Eligibility

Sex
ALL
Min age
12 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria 1. Age ≥12 years old 2. Suspected or confirmed diagnosis of a cardiac mass of any nature as assessed by standard clinical, radiological and/or pathological procedures. Exclusion Criteria 1\. Inability of the pa ent to fully understand and sign the informed consent.

Primary outcome measure(s)

  • Molecular profile — Jul2024-Jul2029
    Collect and analyse blood and tissue samples from both cases and control in terms of molecular profile

Trial sites (1)

FacilityCityRegionStatus
Niguarda Hospital Milan Italia Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07235865 on ClinicalTrials.gov ↗ ← All trials in Italy