Clinical Trials in Italy / NCT07291609
Recruiting Observational

Microplastics and Nanoplastics in Patients With Chronic Coronary Syndromes

NCT07291609 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2025-01-01
Last updated
2026-06-09

Condition(s) studied

Chronic Coronary SyndromeMicroplasticsNanoplasticsCoronary Artery DiseaseCoronary PlaqueComputed TomographyPollution Exposure

Study summary

The CCS-plastics is an investigator-initiated, prospective, multicenter study of patients undergoing coronary CT angiography (CCTA) for suspected or known chronic coronary syndromes (CCS) referred to invasive coronary angiography for clinical indication. Patients identified as eligible for the protocol will be asked for written consent to participate in the study. The patients' dossiers will be uploaded and transmitted to the core laboratory for analysis. The routine management of the CCS patients will not be affected and all patients will be managed according to current standards. Invasive coronary angiography and coronary blood samples will be performed following the current standards, guidelines, and indications. During invasive coronary angiography, coronary blood samples will be collected per standard of care and sent to a centralized, specialized core laboratory for MNPs and biomarkers analysis. The central core lab for MNPs analyses will be the University of Campania Luigi Vanvitelli, Naples, Italy. The identification, quantification (concentration, mcg/ml), and typing of plastic particles will be performed in each tube for each patient, using pyrolysis-gas chromatography-mass spectrometry (Py-GC/MS) and laser direct infrared (LDIR) spectroscopy. The CCTA will be centrally analyzed by Centro Cardiologico Monzino to evaluate qualitative and quantitative plaque features. Patients will be followed clinically at 1 and 3 years per standard of care.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: ALL the following: 1. Age \> 18 years old; 2. Suspected or known chronic coronary syndromes undergoing coronary CT angiography; 3. Clinical indication to invasive coronary angiography; 4. Able to give informed consent. Exclusion Criteria: 1. Coronary CT angiography not available; 2. Poor quality CCTA; 3. Absence of native coronary stenosis \>=50% at CCTA; 4. Contraindications to invasive coronary angiography and percutaneous coronary intervention 5. Life expectancy \< 1 year due to non-cardiac pathology

Primary outcome measure(s)

Trial sites (6)

FacilityCityRegionStatus
Division of Cardiology, A.O.R.N. "Sant'Anna e San Sebastiano", Caserta, Italy. Caserta Italy Not Yet Recruiting
Cardiovascular Division, Morgagni-Pierantoni University Hospital, Forlì, Italy. Forlì Italy Not Yet Recruiting
Centro Cardiologico Monzino Milan Italy Active Not Recruiting
Department of Advanced Medical and Surgical Sciences, University of Campania-Luigi Vanvitelli, Naples, Italy. Naples Italy Active Not Recruiting
Sant'Andrea University Hospital Roma Italy Recruiting
Azienda Ospedaliera Integrata Verona, Italy Verona Italy Recruiting

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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 NCT07291609 on ClinicalTrials.gov ↗ ← All trials in Italy