Registry of patients with acute cardiovascular diseases in Naples
Official title: Naples Federico II Intensive Cardiac Care Unit Registry (Naples FED2-ICCU Registry)
Run by Federico II University · NCT06162247 · Data updated 2026-11-12
This study looks at how patients with serious heart problems are treated and what happens to them while they are in the hospital and after they go home.
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 | November 20, 2023 |
| Main results expected | November 20, 2033 |
| Study ends | November 20, 2033 |
| Registry record updated | March 3, 2025 |
| Trial ID | NCT06162247 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older who are admitted with acute cardiovascular diseases and can provide informed consent.
✕Probably not a fit
Patients who do not consent to data collection 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
This observational study aims to evaluate the current epidemiology, management, and clinical outcomes of patients with acute cardiovascular diseases admitted to the Intensive Cardiac Care Unit (ICCU) at the University of Naples Federico II. It will collect demographic, clinical, procedural, therapeutic, and outcome data from patients who provide informed consent. The study will follow patients during their hospital stay and at subsequent follow-ups to assess clinical outcomes, which will be adjudicated by an independent committee. The data will be anonymized and managed using a secure electronic data capture system.
Why it matters
Potential benefit: If successful, this study could enhance understanding of acute cardiovascular disease management and improve patient outcomes.
How similar studies have gone: Other observational studies in similar settings have shown success in improving clinical outcomes through data collection and analysis.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Acute cardiovascular disease admitted at our ICCU 2. Age ≥18 years; 3. Written informed consent. Exclusion Criteria: 1\) Patients not providing consent to data collection
Where it's running
-
Department of Advanced Biomedical Sciences, University Federico II of Naples
Naples, Italy Recruiting
Study contacts
- Principal investigator: Giuseppe Gargiulo, MD, PhD — Department of Advanced Biomedical Sciences
- Study coordinator: Giuseppe Gargiulo, MD, PhD
- Email: giuseppe.gargiulo1@unina.it
- Phone: +39-7462253
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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This pilot, noninvasive study tests whether the NIRSense wearable can help detect deterioration in adults with cardiogenic shock risk due to heart attack or heart failure.
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Safety and Efficacy of an Extracorporeal Ventricular Assist System for Cardiogenic Shock
This study tests whether an extracorporeal ventricular assist device can safely provide short-term heart support and help patients with cardiogenic shock or trouble weaning from bypass.
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.