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Effect of Cilostazol compared with Clopidogrel about prevention of myocardial injury after elective percutaneous coronary intervention :Prospective,Randomized,Open,Blinded-Endpoint trial

Effect of Cilostazol compared with Clopidogrel about prevention of myocardial injury after elective percutaneous coronary intervention :Prospective,Randomized,Open,Blinded-Endpoint trial - ECARTE trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002351
Enrollment
100
Registered
2010-06-01
Start date
2009-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

ischemic heart disease

Interventions

Patients will be given Aspirin 100mg + cilostazol 200mg orally twice daily. Both drugs will be administered to patients starting seven days or more prior to PCI. Patients will be given Aspirin 100mg o

Sponsors

Department of Cardiology, Nagoya University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients with stable angina (2) Patients who will undergo PCI (Only those who use bare-metal stents)

Exclusion criteria

Exclusion criteria: (1)Patients with unstable angina (2)Patients who use drug-eluting stents (DES) (3)Patients with a medical history of acute myocardial infarction within three months (4)Patients whose levels of CK and CK-MB,troponin-I are above upper limits of normal at the time of consent acquisition (5)Patients taking an anticoagulant (warfarin) (6)Patients who have a medical history of hypersensitivity to cilostazol, aspirin, and/or clopidogrel (7)Patients with thrombocytopenia (8)Patients with hepatic dysfunction (AST (GOT) or ALT(GPT) > 100 IU/L within three months) (9)Patients with renal dysfunction (serum creatinine >2.0mg/dl within three months) (10)Patients with congestive heart failure (11)Patients who are pregnant (12)Patients with bleeding

Design outcomes

Primary

MeasureTime frame
1.Frequency of increase of troponin-I above the upper limit of normal 2.Frequency of increase of CK >2 times above the upper limit of normal 3.Frequency of increase of CK-MB>2 times above the upper limit of normal 4.Average value of cardiac enzymes (CK/CK-MB/troponin-I) 5.Average rate of change of cardiac enzymes (CK/CK-MB/troponin-I)

Countries

Japan

Contacts

Public ContactHideki Ishii

Nagoya University Graduate School of Medicine Department of Cardiology

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026