Registry collecting data on patients undergoing heart artery procedures
Naples PCI Registry
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 |
|---|---|
| Enrollment | 5000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Federico II University Academic / other |
| Locations | 1 site (Naples) |
| Trial ID | NCT05248165 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 and older with clinical evidence of coronary artery disease requiring PCI.
Not a fit: Patients unable to provide informed consent will not benefit from this study.
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 performed: Other registries have successfully documented outcomes of PCI, indicating that this approach is well-established in the field.
Eligibility criteria
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 this trial is running
Naples
- Department of Advanced Biomedical Sciences — Naples, Italy (Recruiting)
Study contacts
- Study coordinator: Giovanni Esposito, MD, PhD
- Email: espogiov@unina.it
- Phone: +390817463075
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.