Registry collecting data on patients undergoing heart artery procedures
Official title: Naples PCI Registry
Run by Federico II University · NCT05248165 · Data updated 2026-11-12
This study is collecting information from patients who are having heart artery procedures to see how they do during and after their treatment.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | Federico II University Academic / other |
| Locations | 1 site (Naples) |
| Status | Recruiting |
| Started | March 1, 2022 |
| Main results expected | March 30, 2032 |
| Study ends | March 30, 2032 |
| Registry record updated | February 23, 2024 |
| Trial ID | NCT05248165 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older with clinical evidence of coronary artery disease requiring PCI.
✕Probably not a fit
Patients unable to provide informed consent will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The Naples PCI Registry aims to gather prospective data on the clinical, laboratory, and angiographic characteristics of patients undergoing percutaneous coronary intervention (PCI) for coronary artery disease. This observational study will follow patients during their hospital stay and at a one-year follow-up to assess various clinical outcomes, including death, myocardial infarction, and other cardiovascular events. The registry will evaluate both stent-based and non-stent-based interventions, with all adverse events independently reviewed by a clinical events committee.
Why it matters
Potential benefit: If successful, this registry could enhance understanding of PCI outcomes and improve patient care in coronary artery disease.
How similar studies have gone: Other registries have successfully documented outcomes of PCI, indicating that this approach is well-established in the field.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Clinical evidence of coronary artery disease requiring PCI; 2. Age ≥18 years; 3. Written informed consent. Exclusion Criteria: 1\. Inability to provide informed consent.
Where it's running
-
Department of Advanced Biomedical Sciences
Naples, Italy Recruiting
Study contacts
- Study coordinator: Giovanni Esposito, MD, PhD
- Email: espogiov@unina.it
- Phone: +390817463075
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.