Clinical Trial

CYP2C19 Genotype-Guided P2Y12 Receptor Inhibitor Selection After Complex Percutaneous Coronary Intervention

Recruiting Phase 4
View on ClinicalTrials.gov →
Summary
In Ease Asia clinical trials, P2Y12 inhibitor (ticagrelor or clopidogrel) monotherapy after 3-month dual antiplatelet therapy (DAPT) resulted in a lower incidence of clinically significant bleeding, without increasing risk of major adverse cardiac and cerebrovascular events, even if acute coronary syndrome (ACS) following complex percutaneous coronary intervention (PCI) when compared with standard DAPT. Although better understood "East Asian Paradox", finding the right CYP2C19 genotype-guided P2Y12 inhibitor selection to balance maintaining ischaemic prevention and less bleeding remains a topic in real-world clinical practice.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-02-21; most recent amendment 2024-03-18.
Trial Details
NCT Number NCT06283888
Lead Sponsor Zunyi Medical College
Conditions ACS - Acute Coronary Syndrome, CYP2C19 Polymorphism
Enrollment 1,200 participants
Start Date 2024-04-01
Primary Completion 2028-04-01 (estimated)
Study Completion 2028-12-01 (estimated)
Updated on ClinicalTrials.gov 2024-03-20