Comparison of Antiplatelet Effect of Ticagrelor vs Tirofiban in Patients With Non-ST Elevation Acute Coronary Syndrome
Launched by PUSAN NATIONAL UNIVERSITY YANGSAN HOSPITAL · Aug 7, 2012
Trial Information
Current as of May 07, 2025
Unknown status
Keywords
ClinConnect Summary
In combination with aspirin, P2Y12 receptor antagonist or glycoprotein IIb/IIIa inhibitor(GPI) is now a recommended drug as the standard dual antiplatelet regimen in patients with acute coronary syndrome(1).
Ticagrelor is a newly developed oral P2Y12 receptor inhibitor. It shows faster, greater and more consistent platelet inhibition as compared with previous P2Y12 receptor antagonist clopidogrel(2) and it also shows better clinical outcome and similar risk for bleeding as compared with clopidogrel(3).Interestingly, pharmacodynamic data of some studies showed excellent effect of ticagrelor...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients with recent or current ischemic symptoms at the time of randomization will be eligible if 2 of the following criteria are met: ST-T change indicating ischemia; a positive test of biomarker indication myocardial necrosis; or one of several risk factors(age ≥60 years
- • Previous myocardial infarction or coronary artery bypass grafting \[CABG\]
- • Coronary artery disease with stenosis of ≥50% in at least two vessels
- • Previous ischemic stroke, transient ischemic attack, carotid stenosis of at least 50%, or cerebral revascularization
- • Diabetes mellitus
- • Peripheral arterial disease; or chronic renal dysfunction, defined as a creatinine clearance of \<60 ml per minute per 1.73 m2 of body surface area)
- Exclusion Criteria:
- • 1. Administration of fibrinolytic or any GP IIb/IIIa inhibitors for the treatment of current AMI
- • 2. Major surgery or trauma within 30 days
- • 3. Active bleeding
- • 4. Previous stroke in the last six months
- • 5. Oral anticoagulant therapy
- • 6. Pre-existing thrombocytopenia
- • 7. Vasculitis
- • 8. Hypertensive retinopathy
- • 9. Severe hepatic failure
- • 10. Severe renal failure requiring hemodialysis
- • 11. Documented allergy/intolerance or contraindication to tirofiban or P2Y12 inhibitor
- • 12. Uncontrolled hypertension (systolic or diastolic arterial pressure \>180 mmHg or 120, respectively, despite medical therapy)
- • 13. Limited life expectancy, e.g. neoplasms, others
- • 14. Inability to obtain informed consent
About Pusan National University Yangsan Hospital
Pusan National University Yangsan Hospital is a leading medical institution dedicated to advancing healthcare through innovative clinical research and patient-centered care. As a sponsor of clinical trials, the hospital leverages its expertise in various medical disciplines to investigate new therapies, improve treatment protocols, and enhance patient outcomes. With a commitment to ethical standards and rigorous scientific methodology, Pusan National University Yangsan Hospital collaborates with multidisciplinary teams to ensure the highest quality of clinical research, contributing significantly to the global medical community and fostering advancements in healthcare.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Yangsan, Kyeongsangnamdo, Korea, Republic Of
Patients applied
Trial Officials
June Hong Kim, MD,PhD
Principal Investigator
Pusan National University Yangsan Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials