CompletedNot Applicable

Culprit-first in Primary Percutaneous Coronary Intervention

Israel106 participantsStarted 2021-05-01

Plain-language summary

The aim of this study is to assess the impact of culprit-first versus culprit-last percutaneous coronary intervention on the door to balloon time and clinical outcomes in patients with ST-elevation myocardial infarction.

Who can participate

Age range18 Years – 120 Years

SexALL

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Inclusion Criteria: * Patients presenting with STEMI who are eligible for PPCI Exclusion Criteria: * Cardiac arrest * Cardiopulmonary resuscitation or extracorporeal membrane oxygenation on arrival to the catheterization laboratory * Prior coronary artery bypass grafting surgery

What they're measuring

Needle-to-balloon time of 10 minutes or less

Timeframe: through study completion, an average of 1 year

Trial details

NCT IDNCT05415085

SponsorShaare Zedek Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-06-30

View on ClinicalTrials.gov More Coronary Artery Disease trials