Clinical Trials Directory

Trials / Terminated

TerminatedNCT02075125

Prasugrel and Ticagrelor in ST-segment Elevation Myocardial Infarction

Comparison of Prasugrel and Ticagrelor Antiplatelet Effects in Korean Patients Presenting With ST-segment Elevation Myocardial Infarction

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
39 (actual)
Sponsor
Dong-A University · Academic / Other
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To compare efficacy and safety of prasugrel and ticagrelor in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention.

Detailed description

Prasugrel and ticagrelor are recommended in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI). Both prasugrel and ticagrelor show more rapid and potent antiplatelet effect compared with clopidogrel. However, previous report comparing the efficacy and safety of prasugrel and ticagrelor in patients with STEMI of East Asian ethnicity is lacking. Therefore, the aim of this study is to compare the antiplatelet efficacy and safety using laboratory platelet function tests and clinical outcomes in patients with STEMI treated with either prasugrel or ticagrelor.

Conditions

Interventions

TypeNameDescription
DRUGPrasugrel 60 mgPatient administer prasugrel 60 mg as loading dose followed by 10 mg/day as maintenance dose.
DRUGTicagrelor 180 mgPatients administer ticagrelor 180 mg as loading dose followed by 90 mg bid as maintenance dose.

Timeline

Start date
2014-01-01
Primary completion
2015-04-01
Completion
2015-04-01
First posted
2014-03-03
Last updated
2017-08-18
Results posted
2016-02-01

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02075125. Inclusion in this directory is not an endorsement.