Myocardial Infarction Clinical Trial
Official title:
Efficacy and Safety of Early Versus Late Loading Dose of Ticagrelol in Patients With ST Segment Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention
Current guidelines recommend percutaneous coronary intervention (PCI) for most patients with
ST segment elevation acute myocardial infarction (STEMI) or with non ST segment elevation
acute coronary syndrome (NSTEACS) . In STEMI patients, PCI is advised in all patients in the
first 12 hours after onset of symptoms, the earlier the better.
This condition is referred to as "no-reflow phenomenon." , no-reflow is defined as suboptimal
myocardial reperfusion through a part of coronary circulation without angiographic evidence
of mechanical vessel obstruction.
Effective antiplatelet therapy combining the inhibition of both thromboxane A2-dependent
platelet aggregation and P2Y12 receptors is necessary in patients undergoing percutaneous
coronary intervention (PCI), particularly those with ST-segment elevation myocardial
infarction (STEMI).
The goal of DAPT (Aspirin and P2Y12 receptor inhibitors) is to reduce the risk of ischemic
events such as (re)-infarction and the risk of stent thrombosis after PCI. It is logical to
assume that early administration of a P2Y12 inhibitor prior to PCI (referred to as
pre-treatment) should provide greater benefit given the fact that even the fastest acting
oral P2Y12 inhibitors take at least 30-60 min.
Various studies and meta-analyses suggested that pretreatment with Clopidogrel in patients
with STEMI could reduce the rate of ischemic events without excess bleeding, but its
effectiveness may be limited by its slow onset of action and the variable response. In
contrast, the new oral P2Y12-receptor antagonists (Prasugrel or Ticagrelol) inhibit platelet
function in less than 1 hour, which is compatible with transfer times for primary PCI.
Ticagrelor is a direct-acting inhibitor of the platelet P2Y12 receptor with a rapid
antiplatelet effect. It has been shown to reduce the rate of major cardiovascular events
among patients with acute coronary syndromes, as compared with Clopidogrel, and has the
potential to improve coronary reperfusion and the prognosis for patients with STEMI treated
with primary PCI. but The issue of pre-treatment with ticagrelor for patients with STEMI
remains an area of ongoing debate; whether they are initiated in the pre-hospital setting,
emergency department, or anywhere .
Status | Not yet recruiting |
Enrollment | 800 |
Est. completion date | April 1, 2021 |
Est. primary completion date | March 1, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: 1. Patients who were diagnosed as STEMI according to criteria developed by the European Society of Cardiology. 2. Onset of maximal intensity of chest pain within 12 hours before procedure. Exclusion Criteria: 1. Contraindication to Ticagrelor (e.g., hypersensitivity, active bleeding, history of previous intracranial hemorrage, moderate to severe hepatic impairment, GI bleeding within the past 6 months, major surgery within past 4 weeks) 2. Patient who has recently received loading dose of Clopidogrel or are on chronic treatment of Clopidogrel. 3. Patients who are on oral anticoagulation therapy that cannot be stopped (i.e., patient with prosthetic valves, chronic AF…etc) 4. Patients with clinically significant thrombocytopenia. 5. Previous enrolment in the present study (Upstream use of GPIIb/IIIa is not recommended as a concomitant treatment) |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Assiut University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The incidence of Major adverse cardiovascular events (MACE) | Efficacy end point | 6 weeks | |
Primary | The occurrence of major or minor bleeding | safety endpoints | 6 weeks |
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