Drug-Coated Balloon Primary PCI in ST-Segment Elevation Myocardial Infarction

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMedical University of Vienna

About this trial

Drug-eluting stent (DES)-based primary percutaneous intervention (pPCI) has been established as the standard of care for patients presenting with ST-segment elevation myocardial infarction (STEMI), having demonstrated superiority over thrombolysis, plain balloon angioplasty, and bare-metal stents. Recently, the use of drug-coated balloons (DCB) has expanded dramatically across a variety of anatomical and clinical settings, including de novo coronary lesions. A DCB-based pPCI strategy may simplify the procedure and mitigate the risks of inadequate stent sizing due to spasm or large thrombus burden, acute stent thrombosis, distal embolization, no reflow, and the relatively higher incidence of late stent-related adverse events compared with elective PCI. Despite these theoretical advantages, data on the safety and efficacy of DCB-based pPCI in STEMI remains limited.

The aim of this registry is to explore procedural and clinical outcomes of patients with STEMI treated with a DCB-based pPCI strategy.

Eligibility criteria

Qualifiers

All ST-elevation MI undergoing Primary PCI

Disqualifiers

In-stent culprit lesion

Contraindications to antiplatelets

Stent implantation within 3 months before enrollment

Cardiac arrest, intubation, or cardiogenic shock

Trial design

Treatments tested in this trial

  • Drug-Coated Balloon

Treatment groups

300 Participants
are divided into 1 treatment group

Sponsors and collaborators