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Clinical outcome of prasugrel compared with clopidogrel

Clinical outcome of prasugrel compared with clopidogrel - Clinical outcome of prasugrel

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000018133
Enrollment
600
Registered
2015-07-01
Start date
2015-07-01
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

None listed

Sponsors

Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with ischemic heart disease who underwent PCI with low-dose aspirin and thienopyridine in Kyoto university hospital between May 2013 and May 2015.

Exclusion criteria

Exclusion criteria: Contraindication of prasugrel or clopidogrel

Design outcomes

Primary

MeasureTime frame
incidence of non-fatal myocardial infarction or stent thrombosis at 30 days

Secondary

MeasureTime frame
all cause death, ischemic stroke, hemorrhagic stroke, any bleeding events or rug allergy.

Countries

Japan

Contacts

Public ContactJunichi Tazaki

Graduate School of Medicine, Kyoto University Department of Cardiovascular Medicine

jun1@kuhp.kyoto-u.ac.jp075-751-3188

Outcome results

None listed

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