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International Survey of Acute Coronary Syndromes (ISACS)

U

University of Bologna

Status

Enrolling

Conditions

Unstable Angina Pectoris
Acute Coronary Syndrome
Myocardial Infarction
Coronary Disease

Study type

Observational

Funder types

Other

Identifiers

NCT01218776
ISACS-TC 1

Details and patient eligibility

About

The International Registry of Acute Coronary Syndromes registry study (ISACS) is both a retrospective and prospective study which was designed in order to obtain data of patients with acute coronary syndromes, and herewith control and optimize internationally guideline-recommended therapies in these countries

Full description

Aims of this survey study are (1) documentation of the characteristics of all patients presenting to the ISACS centers with STEMI or NSTEMI (2) documentation of in-hospital outcome, and outcome rates at 6 month and 1 year, (3) documentation of invasive procedures and procedure-associated complications (4) documentation of therapeutic regimens and investigation conformity of treatment with already established guidelines.

Investigators:

ISACS Administrative Committee:

Raffaele Bugiardini (Italy-Principal Investigator) Lina Badimon (Spain) Olivia Manfrini (Italy- Project Coordinator) Edina Cenko (Italy-Center Coordinator)

Steering Committee:

Mirza Dilic (Bosnia and Herzegovina), Asen Goudev (Bulgaria), Davor Milicic (Croatia), Raffaele Bugiardini, Edina Cenko and Olivia Manfrini (Italy) Gani Bajraktari (Kosovo), Andrejs Erglis and Ilja Zakke (Latvia), Remigius Zaliunas and Olivija Gustiene (Lithuania), Sasko Kedev and Marija Vavlukis (North Macedonia), Mihail Popovici (Moldova), Maria Dorobantu (Romania), Zorana Vasiljevic (Serbia), Eva Goncalvesova and Martin Studenkan (Slovakia) , Alexander N. Parkhomenko (Ukraine) , Christopher P Gale (United Kingdom).

Enrollment

36,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • acute coronary syndromes

Exclusion criteria

  • under age or not able to give informed consent

Trial design

36,000 participants in 1 patient group

Male, Female, Kidney Disease, Elderly
Description:
Non-interventional patient registry

Trial contacts and locations

1

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Central trial contact

Raffaele Bugiardini, MD; Lina Badimon, MD

Data sourced from clinicaltrials.gov

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