ST Segment Elevation Myocardial Infarction Clinical Trial
Official title:
Efficacy of Early Intracoronary Administration of Fasudil Hydrochloride on Myocardial Perfusion in the Primary PCI of ST-elevation Myocardial Infarction: an Prospective, Randomized and Multicenter Trial
The study aims to evaluate whether an early intracoronary administration of Fasudil Hydrochloride during primary PCI of STEMI can improve epicardial and myocardial perfusion as well as clinical outcomes.
Timely reperfusion therapy is the most effective treatment for acute STEMI patients. Primary
PCI has been documented as the best method for restoration of epicardial blood flow.
Nevertheless, recovery of epicardial blood flow does not necessarily equate to a sufficient
reperfusion at myocardial level. Although epicardial TIMI 3 flow could be achieved in the
majority of STEMI patients by contemporary PPCI, it has been well acknowledged that
microvascular obstruction (MVO) is far more prevalent than the epicardial no-reflow
phenomenon and has huge detrimental impact on clinical outcomes.
Routine thrombus aspiration by special catheter during primary PCI has shown negative or even
harmful results in clinical trials. Distal coronary protective devices are also ineffective
to improve myocardial perfusion. On the contrary, peri-procedual administration of several
medications has shown possibilities to reduce MVO. These medications are mostly anti-platelet
agents such as GP IIb/IIIa receptor and microvascular dilators like adenosine, sodium
nitroprusside and verapamil. Theoretically, intracoronary delivery of medications can be more
effective and potentially decrease side effects. Empirical application of aforementioned
agents seems to improve the epicardial flow in patients not achieving TIMI 3 flow after PCI.
However, it is debatable whether early administration of intracoronary medication (meaning
before PCI) may further reduce MVO assuming it could be better to reduce reperfusion injury.
However, this has not been well investigated yet.
Rho-associated protein kinase (Rho kinase) is expressed in many cells, including smooth
muscle cells and vascular endothelial. Activation of Rho kinase leads to increased smooth
muscle intracellular calcium and robust vasoconstriction. Fasudil hydrochloride is a
rho-kinase inhibitor that severs clinically as a potent small vessel dilator, especially in
the field of cerebral circulation. Meanwhile, It has been empirically used in individual
STEMI cases and showed effectiveness in improving coronary flow for PCI therapy. This study
aims to evaluate whether an early intracoronary administration of Fasudil Hydrochloride can
improve myocardial perfusion and clinical outcomes for STEMI patients undergoing primary PCI.
To ensure the complete delivery of agents within coronary, a special-designed targeted
perfusion micro-catheter will be used for drug delivery. Patients in the control arm will be
administrated by intracoronary saline.
For the results, coronary angiography-based index of epical and myocardial perfusion will be
analyzed. MVO will be determined by cardiac magnetic resonance imaging and quantified as the
percentage of left ventricular myocardial mass (% LV). The rate of composite major adverse
cardiac events (MACEs) at 30 days and 6 months since symptom onset will be the clinical
outcomes.
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