Overview
Study of Platelet Function After Administration of Aspirin Versus Lysine Acetylsalicylate in STEMI Patients
Status:
Unknown status
Unknown status
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
Prasugrel and ticagrelor, new P2Y12-ADP receptor antagonists, are associated with greater pharmacodynamic inhibition and reduction of cardiovascular events in patients with an acute coronary syndrome. However, evidence is lacked about the effects of achieving faster and stronger cyclooxygenase inhibition with intravenous lysine acetylsalicylate (LA) compared to oral aspirin on prasugrel inhibited platelets. Recently, we demonstrated in healthy volunteers that the administration of intravenous LA resulted in a significantly reduction of platelet reactivity compared to oral aspirin on prasugrel inhibited platelets. Loading dose of LA achieves platelet inhibition faster, greater and with less variability than aspirin. However, there are no data of this issue in patients with an ST-segment elevation myocardial infarction (STEMI). The ECCLIPSE-STEMI trial will study the effect of LA versus aspirin in platelet reactivity in patients with STEMIPhase:
Phase 2/Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Fundacion Investigacion Interhospitalaria CardiovascularTreatments:
Acetylsalicylic acid lysinate
Aspirin
Criteria
Inclusion Criteria:- Aged > 18.
- Patients with ST-segment myocardial infarction.
- Signed written informed consent.
Exclusion Criteria:
- Known allergies to aspirin, clopidogrel, prasugrel or ticagrelor.
- Cardiogenic shock or hemodinamic instability.
- Recent antiplatelet therapy (<14 days).
- Oral anticoagulation with a coumarin derivative.
- Any active bleeding or blood dyscrasia.
- Recent gastrointestinal bleeding (<6 months prior to inclusion).
- Recent history of stroke, TIA or intracranial bleeding (<6 months prior to inclusion).
- Known anemia, trombopenia or severe chronic kidney/liver disease
- Any known active neoplasm.
- Pregnant females.