Ticagrelor With Low-dose Versus Regular Aspirin in Patients With Acute Coronary Syndrome (ACS) at High-Risk for Ischemia After Percutaneous Coronary Intervention

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorFu Wai Hospital, Beijing, China

About this trial

The present study is aimed to compare the safety and efficacy of Ticagrelor with low-dose Aspirin versus standard dual anti-platelet therapy (DAPT) in patients with acute coronary syndrome (ACS) at high risk for ischemic events after percutaneous coronary intervention (PCI) and stent implantation.

Eligibility criteria

Qualifiers

ACS patients at high risk for ischemic events after successful PCI with implantation of at least one drug eluting stent

Able and willing to provide informed consent and participate in 12 months follow-up period

Able to receive DAPT treatment

Enrollment into the study will require meeting at least one angiographic or clinical inclusion and none of the

Disqualifiers

Family history of premature coronary heart disease (Coronary heart disease in first-degree male relative <55 years old or in first-degree female relative <65 years old)

Repeated myocardial infarction

Positive serum cardiac troponin I/T

Combined with at least one organ/system with atherosclerotic disease (e.g. intracranial or peripheral arteries)

Trial design

Treatments tested in this trial

  • Aspirin
  • Ticagrelor

Treatment groups

1,220 Participants
are divided into 2 treatment groups