Evaluating patients with acute coronary syndrome and myocardial injury
Acute Myocardial Infarction From Clinical Presentation to Strategy Treatment
IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT03883711
This study is collecting information from patients with acute coronary syndrome or heart injury to better understand their conditions and improve future care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 11000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna (other) |
| Locations | 3 sites (Bologna, Bologna and 2 other locations) |
| Trial ID | NCT03883711 on ClinicalTrials.gov |
What this trial studies
This observational study collects data from patients diagnosed with acute coronary syndrome or myocardial injury to enhance understanding of these conditions. It involves both retrospective and prospective data collection from multiple hospitals, focusing on patient characteristics, long-term outcomes, and adherence to treatment guidelines. Information will be gathered from in-hospital medical records, and statistical analyses will be performed to assess outcomes. The study aims to create a comprehensive database to support future research and improve patient care.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old who have been diagnosed with acute coronary syndrome or myocardial injury.
Not a fit: Patients under 18 years old or those unable to provide informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies and outcomes for patients with acute coronary syndrome and myocardial injury.
How similar studies have performed: Other studies focusing on acute coronary syndrome have shown success in improving patient outcomes and treatment adherence, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient aged \> 18 years old * Acute coronary syndrome or myocardial injury * Written informed consent Exclusion Criteria: * under age or not able to give informed consent
Where this trial is running
Bologna, Bologna and 2 other locations
- Policlinico Sant'Orsola-Malpighi, Cardiology Department — Bologna, Bologna, Italy (RECRUITING)
- Ospedale Maggiore Carlo Alberto Pizzardi — Bologna, BO, Italy (RECRUITING)
- Ospedale Morgagni - Pierantoni — Forlì, FC, Italy (RECRUITING)
Study contacts
- Principal investigator: Carmine Pizzi, Dr — University of Bologna, Cardiology Department
- Study coordinator: Carmine Pizzi, Prof
- Email: carmine.pizzi@unibo.it
- Phone: 0039 (0)512144933
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.
Conditions: Acute Coronary Syndrome, Myocardium, Injury, Acute coronary syndrome, Myocardial injury, ACS, MINOCA