The ELECTRA pilot study is a randomized, open-label, pharmacokinetic and pharmacodynamic trial designed to evaluate the effect of ticagrelor maintenance dose reduction on platelet inhibition in stable patients who recently underwent acute myocardial infarction and were treated with percutaneous coronary intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
52
Ticagrelor 90 mg twice daily
Ticagrelor 60 mg daily
Cardiology Department, Dr. A. Jurasz University Hospital
Bydgoszcz, Kuyavian-Pomeranian Voivodeship, Poland
Platelet Reactivity Assessed with the VASP assay
Platelet inhibition evaluated with the VASP assay 45 days after myocardial infarction.
Time frame: 45 days
Platelet Reactivity Assessed with Multiple Electrode Aggregometry
Platelet inhibition evaluated with Multiple Electrode Aggregometry 45 days after myocardial infarction.
Time frame: 45 days
Number of Patients With High Platelet Reactivity according to the VASP assay
Number of Patients With High Platelet Reactivity according to the VASP assay 45 days after myocardial infarction.
Time frame: 45 days
Number of Patients With High Platelet Reactivity according to Multiple Electrode Aggregometry
Percentage of Patients With High Platelet Reactivity according to Multiple Electrode Aggregometry 45 days after myocardial infarction.
Time frame: 45 days
Plasma concentration of Ticagrelor
Evaluation of ticagrelor plasma concentration 45 days after myocardial infarction.
Time frame: 45 days
Plasma concentration of AR-C124910XX
Evaluation of ticagrelor active metabolite plasma concentration 45 days after myocardial infarction.
Time frame: 45 days
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