Actively Recruiting

Age: 18Years +
All Genders
ID01218776

International Survey of Acute Coronary Syndromes

Led by University of Bologna · Updated on 2025-04-16

36000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting the International Survey of Acute Coronary Syndromes (ISACS), an observational study designed to collect and analyze data from patients with acute coronary syndromes such as STEMI or NSTEMI. The study aims to document patient characteristics, in-hospital outcomes, and longer-term results at 6 months and 1 year. It also assesses invasive procedures, complications, and how well treatments follow established guidelines internationally. This study is non-interventional and serves as a patient registry. It collects detailed information from participating centers on treatment regimens and procedures without administering any specific therapies. The study covers both retrospective and prospective data gathering, focusing on outcomes and adherence to recommended care practices across multiple countries. Participants provide data through hospital records and follow-up evaluations at 30 days, 6 months, and 1 year. Researchers measure outcomes including all-cause mortality, cardiovascular deaths, recurrent heart attacks, and genetic studies related to clinical results. Adherence to guideline-recommended therapies is also monitored. The study is led by the University of Bologna and involves various international collaborators, with patient participation lasting up to one year after initial admission.

CONDITIONS

Brief Title

International Survey of Acute Coronary Syndromes

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of acute coronary syndromes such as STEMI or NSTEMI
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Unable to give informed consent

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Hospital stay duration

Participants diagnosed with acute coronary syndromes such as STEMI or NSTEMI are documented including invasive procedures and complications.

1 hospital admission visit

Surveillance

Duration - Up to 1 year

Participants are observed to document in-hospital outcomes and outcomes at 6 months and 1 year including mortality, recurrent myocardial infarction, and adherence to guideline-recommended therapies.

Visits or contacts at discharge, 6 months, and 1 year

Trial Site Locations

Total: 1 location

1

University of Bologna

Bologna, Emilia-Romagna, Italy, 40138

Actively Recruiting

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Research Team

R

Raffaele Bugiardini, MD

L

Lina Badimon, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Unfractionated heparin-clopidogrel combination in ST-elevation myocardial infarction not receiving reperfusion therapy.

Raffaele Bugiardini, Maria Dorobantu, Zorana Vasiljevic...

https://pubmed.ncbi.nlm.nih.gov/25988359

Factors associated with use of percutaneous coronary intervention among elderly patients presenting with ST segment elevation acute myocardial infarction (STEMI): Results from the ISACS-TC registry.

Lucian Câlmâc, Vlad Bătăilă, Beatrice Ricci...

https://pubmed.ncbi.nlm.nih.gov/27381859

The International Survey of Acute Coronary Syndromes in Transitional Countries (ISACS-TC): 2010-2015.

Raffaele Bugiardini, Lina Badimon, ISACS-TC Investigators and Coordinators

https://pubmed.ncbi.nlm.nih.gov/27386758