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Dual antiplatelet therapy with ticagrelor and acetylsalicylic acid (ASA) vs. ASA only after isolated coronary artery bypass grafting in patients with acute coronary syndrome (TACSI trial)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-508551-40-00
Acronym
TACSI-01
Enrollment
2200
Registered
2024-10-23
Start date
2018-06-08
Completion date
Unknown
Last updated
2024-12-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary artery multi-vessel disease and left main stenosis

Brief summary

A composite endpoint of the time to all cause death, or myocardial infarction, or stroke, or new coronary revascularization within 12 months

Detailed description

Time to all cause death, Time to all cause death, myocardial infarction or stroke, Time to cardiovascular death, Time to first myocardial infarction, Time to first stroke, Time to new revascularization, Time to coronary angiography, Time to hospitalization for heart failure, Time to cardiovascular hospitalization, Time to sudden death or aborted cardiac arrest, Time to new-onset AF

Interventions

DRUGACETYLSALICYLIC ACID
DRUGTICAGRELOR

Sponsors

Vaestra Goetalandsregionen
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
A composite endpoint of the time to all cause death, or myocardial infarction, or stroke, or new coronary revascularization within 12 months

Secondary

MeasureTime frame
Time to all cause death, Time to all cause death, myocardial infarction or stroke, Time to cardiovascular death, Time to first myocardial infarction, Time to first stroke, Time to new revascularization, Time to coronary angiography, Time to hospitalization for heart failure, Time to cardiovascular hospitalization, Time to sudden death or aborted cardiac arrest, Time to new-onset AF

Countries

Denmark, Finland, Iceland, Norway, Sweden

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026