Skip to content

Ticagrelor monotherapy after coronary stenting in patients with acute myocardial infarction - A prospective single-centre, single-arm phase II study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-514224-17-00
Acronym
5.1
Enrollment
200
Registered
2024-06-11
Start date
2021-12-03
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

Myocardial infarction

Brief summary

The composite of cardiac death, spontaneous myocardial infarction or definite or probable stent thrombosis within 3 months.

Detailed description

Time to the following outcomes at 3- and 12 months (unless specified): Bleeding Academic Research Consortium (BARC) types 3 or 5 bleeding (time-to-event), Definite or probable stent thrombosis or spontaneous target vessel myocardial infarction (time-to-event), Any spontaneous myocardial infarction (time-to-event), All-cause mortality (time-to-event), The composite of cardiac death, spontaneous target vessel myocardial infarction or definite or probable stent thrombosis within 12 months., Platelet reactivity as assessed by the ADP-test (multiplate), at 24 hours and 3 months.

Interventions

Sponsors

Vaestra Goetalandsregionen, Vaestra Goetalandsregionen
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The composite of cardiac death, spontaneous myocardial infarction or definite or probable stent thrombosis within 3 months.

Secondary

MeasureTime frame
Time to the following outcomes at 3- and 12 months (unless specified): Bleeding Academic Research Consortium (BARC) types 3 or 5 bleeding (time-to-event), Definite or probable stent thrombosis or spontaneous target vessel myocardial infarction (time-to-event), Any spontaneous myocardial infarction (time-to-event), All-cause mortality (time-to-event), The composite of cardiac death, spontaneous target vessel myocardial infarction or definite or probable stent thrombosis within 12 months., Platelet reactivity as assessed by the ADP-test (multiplate), at 24 hours and 3 months.

Countries

Sweden

Outcome results

None listed

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