Evaluation of Safety and Efficacy of Two Ticagrelor-based De-escalation Antiplatelet Strategies in Acute Coronary Syndrome

PHASE3UnknownINTERVENTIONAL
Enrollment

4,500

Participants

Timeline

Start Date

February 7, 2022

Primary Completion Date

June 30, 2024

Study Completion Date

June 30, 2024

Conditions
STEMINSTEMIUnstable Angina
Interventions
DRUG

Ticagrelor 90mg

Up to day 30 after ACS, all enrolled patients will receive standard-dose ticagrelor 2x90mg as a part of dual antiplatelet therapy. Participants in SDTA arm will continue treatment with ticagrelor 2x90mg until 12 months post-ACS, while patients in LDTA and LDTP will be switched to low-dose ticagrelor 2x60 mg starting on day 31.

DRUG

Ticagrelor 60mg

Starting from day 31, LDTA and LDTP patients will receive low-dose ticagrelor 2x60mg until 12 months post-ACS.

DRUG

Aspirin

Up to day 90 after ACS, all enrolled patients will receive aspirin 1x100mg as a part of dual antiplatelet therapy. Starting from day 91, LDTP patients will discontinue aspirin and proceed with low-dose ticagrelor monotherapy until 12 months post-ACS, while patients in LDTA and SDTA will continue aspirin 1x100 mg until 12 months post-ACS.

Trial Locations (1)

Unknown

RECRUITING

Antoni Jurasz University Hospital No. 1, Bydgoszcz

Sponsors
All Listed Sponsors
collaborator

Medical Research Agency, Poland

OTHER_GOV

lead

Collegium Medicum w Bydgoszczy

OTHER

NCT04718025 - Evaluation of Safety and Efficacy of Two Ticagrelor-based De-escalation Antiplatelet Strategies in Acute Coronary Syndrome | Biotech Hunter | Biotech Hunter