Survey of patients with acute coronary syndromes
Official title: International Survey of Acute Coronary Syndromes
Run by University of Bologna · NCT01218776 · Data updated 2026-11-12
This study is looking to gather information from patients with heart problems like unstable angina and heart attacks in Eastern Europe to see how they are treated and how they do over time.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 36000 (estimated) |
| Sponsor | University of Bologna Academic / other |
| Locations | 1 site (Bologna, Emilia-Romagna) |
| Status | Recruiting |
| Started | September 28, 2010 |
| Main results expected | December 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | April 16, 2025 |
| Trial ID | NCT01218776 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals diagnosed with acute coronary syndromes.
✕Probably not a fit
Patients under the age of consent or those 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
This observational study aims to collect data on patients presenting with acute coronary syndromes, including unstable angina and myocardial infarction, across various centers in Eastern Europe. It will document patient characteristics, in-hospital outcomes, and treatment regimens to assess adherence to established guidelines. The study will also evaluate the complications associated with invasive procedures and track patient outcomes at six months and one year post-treatment.
Why it matters
Potential benefit: If successful, this study could enhance the management and treatment of acute coronary syndromes by optimizing adherence to clinical guidelines.
How similar studies have gone: Other studies focusing on acute coronary syndromes have shown success in improving treatment outcomes through similar data collection and analysis approaches.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * acute coronary syndromes Exclusion Criteria: * under age or not able to give informed consent
Where it's running
-
University of Bologna
Bologna, Emilia-Romagna, Italy Recruiting
Study contacts
- Principal investigator: Raffaele Bugiardini, MD — University of Bologna
- Study coordinator: Raffaele Bugiardini, MD
- Email: raffaele.bugiardini@unibo.it
- Phone: +39 335 5612962
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Freesolve resorbable magnesium scaffold vs. Xience stent for up to two new heart artery lesions
This trial tests whether the Freesolve resorbable magnesium scaffold works as well as the Xience drug-eluting stent for treating up to two new coronary artery lesions in adults.
-
Healthy Nordic diet's effects on heart disease
This study is testing if following a Healthy Nordic diet can help people with coronary heart disease improve their heart health over 18 months.
-
Single versus dual antiplatelet therapy after drug-coated balloon angioplasty in elderly or high-bleeding-risk patients
This study tests whether taking one antiplatelet medicine is as safe and causes less bleeding than taking two medicines for people aged 75 or older, or adults at high bleeding risk, after drug-coated balloon angioplasty for coronary artery disease.
-
Understanding sex hormones and inflammation in heart disease
This study looks at how sex hormones and inflammation affect heart disease in women to better understand their unique risks and improve treatment.
-
Effects of Dapagliflozin on Heart Health in Patients with Acute Coronary Syndromes
This study is testing if dapagliflozin, a diabetes medication, can improve heart health in people who have just had a heart attack.
-
Using magnetocardiography to identify heart attacks
This study is testing if a new noninvasive heart scan method can help doctors better identify heart attacks in people with chest pain and healthy volunteers.
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.