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Safety of Ticagrelor Monotherapy After Primary Percutaneous Coronary Intervention for ST-elevation Myocardial Infarction and the Effect on Intramyocardial Haemorrhage
Sponsor: Radboud University Medical Center
Summary
The main goal of this clinical trial is to assess whether direct omission of aspirin after Percutaneous Coronary Intervention (PCI) with the continuation of ticagrelor monotherapy for 12 months versus 12 months ticagrelor plus aspirin is equally safe regarding the incidence of ischemic events in patients with ST elevation myocardial infarction (STEMI). Furthermore, the two treatment strategies will be compared regarding the incidence and extent of intramyocardial haemorrhage (IMH) and infarct size in the first week after PCI as determined with Cardiac Magnetic Resonance (CMR). The secondary efficacy endpoint consists of clinical bleeding events and all-cause mortality. The main analyses will comprise of clinical outcomes in the first three months after primary PCI and of CMR results. In addition, we will report on clinical outcomes at thirteen months.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
200
Start Date
2023-07-06
Completion Date
2025-12-01
Last Updated
2024-09-23
Healthy Volunteers
No
Conditions
Interventions
Ticagrelor
Ticagrelor monotherapy for 12 months
Aspirin
Dual antiplatelet therapy (aspirin plus ticagrelor) for 12 months
Locations (5)
Noordwest Ziekenhuisgroep Alkmaar
Alkmaar, Netherlands
Amsterdam UMC
Amsterdam, Netherlands
Rijnstate
Arnhem, Netherlands
Medisch Spectrum Twente
Enschede, Netherlands
Radboudumc
Nijmegen, Netherlands