About this trial
As an effective treatment for acute ST-segment elevation myocardial infarction (STEMI), early reperfusion may reduce the infarct size and improve the prognosis of patients. However, it remains uncertain whether adjunctive thrombolytic therapy administered immediately prior to primary percutaneous coronary intervention (PCI) improves outcomes in patients undergoing the procedure within 120 minutes.
In this investigator-initiated, prospective, multi-center, randomized, double-blind, placebo-controlled trial, subjects meeting the inclusion/exclusion criteria should be randomly assigned 1:1 to the trial group (r-SAK) or the control group (placebo). The risk of major adverse cardiovascular events within 90 days will be observed.
Eligibility criteria
Qualifiers
Age 18-75 years, weight ≥45 kg
Diagnosed as STEMI (meeting the following two conditions simultaneously)
Ischemic chest pain lasts ≥ 30 minutes
ECG indicates that ST-segment elevation of two or more contiguous precordial leads ≥ 0.1 mV, or ST-segment elevation of two or more contiguous precordial leads ≥ 0.2 mV
Disqualifiers
Cardiogenic shock
Active bleeding or known at high risk of bleeding (including grade Ⅲ or Ⅳ retinopathy or retinal gastrointestinal or urinary tract hemorrhage within the past 1 month)
Ischemic stroke or TIA in the past 6 months
History of hemorrhagic stroke
Trial design
Treatments tested in this trial
- Recombinant staphylokinase
- Placebo