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Primary Angioplasty for STEMI During COVID-19 Pandemic (ISACS-STEMI COVID-19) Registry

International Study on Acute Coronary Syndromes - ST-segment Elevation Myocardial Infarction COVID 19

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04412655
Acronym
ISACS-STEMI
Enrollment
6609
Registered
2020-06-02
Start date
2020-05-05
Completion date
2020-06-02
Last updated
2020-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ST Elevated Myocardial Infarction Undergoing Mechanical Reperfusion

Brief summary

The ISACS STEMI COVID-19 has been established in response to the emerging outbreak of COVID-19 to provide a European overview to estimate the real impact of COVID-19 pandemic on treatment and outcome of STEMI by primary angioplasty, and to identify any potential category of patients at risk for delay to treatment or no presentation.

Detailed description

This is a retrospective multicenter registry including at least 40 European primary PCI centers with \> 120 primary PCI/year (with expected average \> 10/month), with the case load of STEMI not expected to be affected by a potential planned reorganization of the STEMI network. The inclusion period will be of 2 months (from March 1st until April 30th). The data will be compared with those retrospectively collected in the same time window of 2019. Inclusion criteria: STEMI treated by primary angioplasty. Primary study outcome: Number of STEMI patients undergoing primary angioplasty. Secondary study outcomes: Ischemia time and the number of late presenters (\> 12 hours from symptoms onset); 3) Door-to-balloon time and the number of patients with a DTB \> 30 minutes); 4) In-Hospital mortality. Data Collection: Data will be collected anonymized through a dedicated CRF. Each center will identify a local Principal Investigator. We will collect information on the study center, demographic, clinical, procedural data. Furthermore, we will collect data on total ischemia time, door-to-balloon time, type of access to the emergency system, COVID positivity, PCI procedure, data on in-hospital mortality.

Interventions

DEVICEPercutaneous Coronary Revascularization for STEMI

Percutaneous Mechanical Reperfusion for STEMI

Sponsors

Università degli Studi del Piemonte Orientale Amedeo Avogadro
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

STEMI Patients undergoing mechanical reperfusion \-

Design outcomes

Primary

MeasureTime frameDescription
Number of patients undergoing primary angioplasty later than 12 hours from symptoms onset;March April 2019 and 2020Number of patients undergoing primary angioplasty later 12 hours from symptoms onset;
Number of patients undergoing primary angioplasty later than 30 minutes from PCI hospital admissionMarch April 2019 and 2020Number of patients undergoing primary angioplasty later than 30 minutes from PCI hospital admission
In-hospital mortalityMarch April 2019 and 2020In-Hospital mortality
Number of patients undergoing primary angioplastyMarch April 2019 and 2020Number of patients undergoing primary angioplasty

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026