Correlation between High Platelet Reactivity with Loading Dose of Prasugrel and Clinical Outcome in the Patients with Acute Coronary Syndrome

Correlation between High Platelet Reactivity with Loading Dose of Prasugrel and Clinical Outcome in the Patients with Acute Coronary Syndrome - Correlation between High Platelet Reactivity with Loading Dose of Prasugrel and Clinical Outcome in the Patients with Acute Coronary Syndrome

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000029729

Enrollment

100

Registered

2017-12-01

Start date

2017-12-01

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

acute coronary syndrome

Interventions

Prasugrel 20mg

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (a) patients with acute coronary syndrome to whom emergent PCI is planned. (b)patients aged over 20 and under 90 years old.

Exclusion criteria

Exclusion criteria: (a) patients wiht bleeding tendency (b) patients with allagy against thienopyridine drugs (c)patients who are not suitable for this study

Design outcomes

Primary

Measure	Time frame
composite of all death, myocardial death, myocardial infarction, stroke, ventricular arrhythmia needing defibrillation, cardiac rupture and serious hemorrhage within 30 days of onset	—

Secondary

Measure	Time frame
composite of all death, myocardial death, myocardial infarction, stroke, heart-failure hospitalization, target lesion revascularization and serious hemorrhage within one year of onset	—

Countries

Japan

Contacts

Public Contactyusuke kawai

Okayama City Hospital Department of Cardiovascular Medicine

jamkuhta@yahoo.co.jp086-737-3000

Outcome results

None listed

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