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Effects of Optimized Antiplatelet Treatment After Percutaneous Coronary Intervention

Pilot Study of Personal Optimized Antiplatelet Treatment After Percutaneous Coronary Intervention in Patients With Acute Coronary Syndromes

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00404781
Enrollment
305
Registered
2006-11-29
Start date
2006-06-30
Completion date
2007-06-30
Last updated
2009-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndromes, Ischemic Heart Disease

Keywords

ischemic heart disease, acute coronary syndromes, percutaneous transluminal coronary angioplasty, platelet function, aspirin, clopidogrel, cilostazol

Brief summary

Effects of dual antiplatelet therapy with aspirin and clopidogrel after percutaneous coronary intervention has been proven. However, patients with low response to those agents are reported be associated with adverse clinical outcomes. We suppose that optimized antiplatelet therapy for individual patients based on platelet function assay may improve long-term outcomes especially in patients with high risk of thrombosis. In this prospective randomized study, patients in control group all receive standard dual antiplatelet therapy, and patients in optimized group receive different antiplatelet therapy according to risk stratification.

Interventions

DRUGcilostazol in addition to aspirin and clopidogrel

Sponsors

Shenyang Northern Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
35 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* non-ST-segment elevated acute coronary syndromes * patients undergoing selective or emergent PCI

Exclusion criteria

* administration of clopidogrel or ticlopidine within 2 weeks * ST-segment elevated myocardial infarction * contraindications of antiplatelet therapy * history of intracranial bleeding * known bleeding disorders * severe liver or kidney disease

Design outcomes

Primary

MeasureTime frame
Major adverse cardiac and cerebral events at 1 year1 year

Secondary

MeasureTime frame
Hemorrhage events at 1 year1 year

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026