University of Bologna
Bologna, Emilia-Romagna, 40138, Italy
Location status: Recruiting
Location contact
Lina Badimon, MD
CONTACT
Raffaele Bugiardini, MD
CONTACT
Raffaele Bugiardini, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT01218776
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
Interested in participating?
Request Info18 year and older
All sexes
Observational
Bologna, Emilia-Romagna, 40138, Italy
Location status: Recruiting
Lina Badimon, MD
CONTACT
Raffaele Bugiardini, MD
CONTACT
Raffaele Bugiardini, MD
PRINCIPAL_INVESTIGATOR
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).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 30 days, 6 months, 1 year
All causes mortality
Time frame: 30 days, 6 months, 1 year
Cardiovascular mortality
Time frame: 30 days, 6 months, 1year
Recurrent myocardial infarction
Time frame: 6 month, 1 year
Pharmacogenetic and cardiovascular genetic studies associated to clinical outcomes
Time frame: discharge, 6 months, 1 year
Adherence to internationally guideline recommended therapies across the participating
Contact information is provided by the study sponsor or research team.
Lina Badimon, MD
CONTACT
Raffaele Bugiardini, MD
CONTACT
University of Bologna
Other
Acronym: ISACS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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