Coronary disease & ACS

Prehospital treatment with zalunfiban (RUC-4) in patients with ST‐ elevation myocardial infarction undergoing primary percutaneous coronary intervention: Rationale and design of the CELEBRATE trial

Am Heart JPublished Rationale and design of a randomised controlled trial

Study context

Population
Patients with ST-elevation myocardial infarction (STEMI) intended to undergo primary percutaneous coronary intervention (PCI)target
Participants
2,499 patients
Planned comparison
Prehospital subcutaneous zalunfiban (2 doses) vs placebo, in addition to standard of care
Primary endpoint
Ranked 7-point scale on clinical outcomes (efficacy); severe or life-threatening GUSTO bleeding (safety)
Methodological detailsCELEBRATE, phase 3, double-blinded, placebo-controlled, international, 1:1:1 randomisation, ongoing
  • CELEBRATE
  • Phase 3
  • Double-blinded
  • Placebo-controlled
  • International
  • 1:1:1 randomisation
  • Ongoing

No results yet. This paper sets out the design of a trial; its results are to come.

Original publication

Prehospital treatment with zalunfiban (RUC-4) in patients with ST‐ elevation myocardial infarction undergoing primary percutaneous coronary intervention: Rationale and design of the CELEBRATE trial. Am Heart J. Published 31 December 2022. doi:10.1016/j.ahj.2022.12.015

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