Naples PCI Registry
Condition(s) studied
Investigational drug(s) / intervention(s)
PCI: Percutaneous coronary intervention
Study summary
The aim of the Naples PCI registry is to collect prospective data on baseline clinical, laboratory, and angiographic characteristics of patients undergoing PCI for acute or chronic coronary artery disease. All patients receive clinical follow-up at hospital discharge and at 1-year follow-up with the objective to assess clinical outcomes, including death, cardiovascular death, myocardial infarction, stroke, stent thrombosis, target-lesion and target-vessel revascularization, contrast-induced acute kidney injury, and bleeding events.
Eligibility
Primary outcome measure(s)
- Number of patients with death — 12 months
Death - Number of patients with myocardial infarction — 12 months
Myocardial infarction - Number of patients with stroke — 12 months
Stroke - Number of patients with stent thrombosis — 12 months
Stent thrombosis - Number of patients with target-vessel revascularization — 12 months
Target vessel revascularization - Number of patients with target-lesion revascularization — 12 months
Target lesion revascularization - Number of patients with contrast-induced acute kidney injury — 12 months
Contrast-induced acute kidney injury - Number of patients with bleeding — 12 months
Bleeding
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of Advanced Biomedical Sciences | Naples | Italy | Recruiting |
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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 NCT05248165 on ClinicalTrials.gov ↗ ← All trials in Italy