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RECRUITING
NCT05986968
NA

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

View on ClinicalTrials.gov

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

Interventions

DRUG

Ticagrelor

Ticagrelor monotherapy for 12 months

DRUG

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