Clinical Trials Directory

Trials / Completed

CompletedNCT02808767

Comparison of Prasugrel and Ticagrelor in the Treatment of Acute Myocardial Infarction

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
1,226 (actual)
Sponsor
Faculty Hospital Kralovske Vinohrady · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the efficacy of Prasugrel and Ticagrelor in the treatment of acute myocardial infarction.

Detailed description

Study objectives: 1. Compare the efficacy and safety of prasugrel and ticagrelor in acute myocardial infarction treated with emergent PCI. 2. Assess the safety of switching to clopidogrel after remission of the acute phase of MI in patients for whom economic barriers do not allow to continue treatment with prasugrel or ticagrelor. All randomized patients with acute myocardial infarction have been treated with standard therapeutic procedures in accordance with the guidelines of European Society of Cardiology (ESC). Participation of patients in the study is not connected to any deviations from the ESC guidelines recommendations.

Conditions

Interventions

TypeNameDescription
DRUGPrasugrelPrasugrel 60 mg loading dose and 10mg/5mg once daily maintenance dose
DRUGTicagrelorTicagrelor 180 mg loading dose and 90 mg twice daily maintenance dose

Timeline

Start date
2013-01-01
Primary completion
2016-05-01
Completion
2017-05-01
First posted
2016-06-22
Last updated
2017-08-11

Locations

1 site across 1 country: Czechia

Source: ClinicalTrials.gov record NCT02808767. Inclusion in this directory is not an endorsement.