Clinical Trials Directory

Trials / Unknown

UnknownNCT02422888

Reducing Micro Vascular Dysfunction in Acute Myocardial Infarction by Ticagrelor

Reducing Micro Vascular Dysfunction In Revascularized ST-elevation Myocardial Infarction Patients by Off-target Properties of Ticagrelor

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
110 (actual)
Sponsor
Amsterdam UMC, location VUmc · Academic / Other
Sex
All
Age
18 Years – 74 Years
Healthy volunteers
Not accepted

Summary

The current trial will compare the protective effect of ticagrelor and prasugrel on microvascular dysfunction in patients with revascularized ST elevation myocardial infarction.

Detailed description

Coronary microvascular dysfunction is highly prevalent in revascularized ST-elevation myocardial infarction and has important prognostic implications. Current data suggest that ticagrelor might be superior to prasugrel in the reduction of coronary microvasculature dysfunction. Thus, we have designed a clinical trial that will compare microvascular function in revascularized ST-elevation myocardial infarction patients at treatment steady state with ticagrelor or prasugrel. Coronary microvascular dysfunction will be assessed with the index of microcirculatory resistance after primary percutaneous coronary intervention and at 1 month follow-up in the infarct-related vessel and non-infarct related vessel.

Conditions

Interventions

TypeNameDescription
DRUGTicagrelorAfter a standard loading dose of 180 mg ticagrelor in the ambulance (before primary PCI), patients will receive a maintenance dose of ticagrelor 90 mg twice a day for 1 year.
DRUGPrasugrelAfter a standard loading dose of 180 mg ticagrelor in the ambulance (before primary PCI), patients will receive a single loading dose of prasugrel 60 mg (1 day after standard loading dose ticagrelor),followed by a maintenance dose of prasugrel 10 mg once a day for 1 year.

Timeline

Start date
2015-05-01
Primary completion
2017-10-01
Completion
2019-10-01
First posted
2015-04-21
Last updated
2018-05-03

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT02422888. Inclusion in this directory is not an endorsement.