Clinical Trials Directory

Trials / Completed

CompletedNCT01531114

PraSugrel vs TicagrElor in ST-Elevation Myocardial Infarction paTients With Diabetes Mellitus

Prasugrel Or Ticagrelor In ST-Elevation Myocardial Infarction Patients With Diabetes Mellitus

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Gennaro Sardella · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Dual antiplatelet therapy is essential in patients following ST-Elevation myocardial infarction (STEMI) with percutaneous coronary intervention (PCI) and drug eluting stent implantation. Current guidelines recommend prasugrel and ticagrelor in patients with STEMI undergoing primary PPCI. We sought to investigate the superiority antiplatelet effect in terms of PR level of loading dose (LD) of Prasugrel (60 mg) versus LD of Ticagrelor (180 mg) in diabetic patients with STEMI undergoing primary PCI at 1 and 2 hours post drug administration. Secondary end-points will be: PR level measured at 6 and 12 hours post study drugs administrationin hospital. All consecutive diabetic patients with STEMI undergoing PPCI with stent implantation will be considered for PR assessment at 1-2-6-12 h after the drug LD administration. All patients must will be naïve for platelet P2Y12 receptor inhibition therapy. A subanalysis will be performed between two study groups according to insulin treatment.

Conditions

Interventions

TypeNameDescription
DRUGticagrelorPatients will be randomized to this arm to receive loading dose of ticagrelor
DRUGprasugrelPatients will be randomized to this arm to receive loading dose of prasugrel

Timeline

Start date
2013-05-01
Primary completion
2015-07-01
Completion
2015-07-01
First posted
2012-02-10
Last updated
2017-06-28

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT01531114. Inclusion in this directory is not an endorsement.