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
| Type | Name | Description |
|---|---|---|
| DRUG | Prasugrel 60 mg | Patient administer prasugrel 60 mg as loading dose followed by 10 mg/day as maintenance dose. |
| DRUG | Ticagrelor 180 mg | Patients 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.