Registry of Acute Coronary Syndromes in Ferrara
Acute coRonary sYndrOmes proSpective regisTry Of Ferrara
This study is collecting information about how patients with acute coronary syndromes are treated in Ferrara, Italy, to better understand their care and outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital of Ferrara Academic / other |
| Locations | 1 site (Cona, Ferrara) |
| Trial ID | NCT02438085 on ClinicalTrials.gov |
What this trial studies
This registry aims to describe the clinical epidemiology and management of acute coronary syndromes (ACS) in Ferrara, Italy. It will collect data on patients admitted to hospitals in the area who receive coronary artery angiography and percutaneous coronary intervention (PCI). The study will gather information on patient characteristics, clinical management, biomarkers, procedural details, and long-term outcomes. The University Hospital of Ferrara serves as the hub center for this initiative, ensuring a high volume of ACS cases for comprehensive analysis.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 years old who are residents of the Ferrara area and are admitted to the hospital for acute coronary syndromes.
Not a fit: Patients who are not residents of the Ferrara area or those under 18 years old will not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could enhance understanding of ACS management and improve patient outcomes in the Ferrara region.
How similar studies have performed: Other similar registries have shown success in improving clinical outcomes and understanding of acute coronary syndromes, indicating that this approach is well-established.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * age \>18 years * hospital admission for acute coronary syndromes * resident in the Ferrara area Exclusion Criteria: * none
Where this trial is running
Cona, Ferrara
- University Hospital of Ferrara — Cona, Ferrara, Italy (Recruiting)
Study contacts
- Study coordinator: Veronica Lodolini, BSc
- Email: veronica.lodolini@student.unife.it
- Phone: +390532236450
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.