Different LD of Ticagrelor for Antiplatelet Effect in Patients With Non-ST-segment Elevation ACS … (NCT01962428) | Clinical Trial Compass
CompletedPhase 4
Different LD of Ticagrelor for Antiplatelet Effect in Patients With Non-ST-segment Elevation ACS Undergoing PCI
China250 participantsStarted 2014-06
Plain-language summary
It is designed to test the hypothesis that high loading dose(360mg) ticagrelor versus conventional loading dose(180mg) will result in a higher inhibition of platelet aggregation(IPA) without increasing the bleeding events.
Who can participate
Age range18 Years – 80 Years
SexALL
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Inclusion Criteria:
* Provision of informed consent prior to any study specific procedures.
* Male or non-pregnant female; aged from 18 to 80 years old.
* Patients with non-ST-segment elevation acute coronary syndromes who were scheduled to undergoing PCI.
Exclusion Criteria:
* Any contraindication against the use of ticagrelor.
* On treatment with a P2Y12 receptor antagonist in past 30 days.
* Known allergies to aspirin or ticagrelor.
* On treatment with oral anticoagulant (Vitamin K antagonists, dabigatran, rivaroxaban).
* Known blood dyscrasia or bleeding diathesis.
* ST-segment elevation acute myocardial infarction.
* Non-ST segment elevation acute coronary syndrome with high-risk features warranting emergency coronary angiography.
* Left ventricular ejection fraction ≤30%; renal failure with creatinine 3 mg/dl; history of liver disease; an increased risk of bradycardia, and concomitant therapy with drugs interfering with CYP3A4 metabolism.
What they're measuring
1
Platelet Reactivity Index(PRI) Measured by VASP-P
Timeframe: 2 hours after the loading dose of ticagrelor
Trial details
NCT IDNCT01962428
SponsorGeneral Hospital of Chinese Armed Police Forces