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Prasugrel Monotherapy Reduced dose in Acute and Chronic Coronary Syndrome Patients after Percutaneous Coronary Intervention

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-520351-24-00
Enrollment
300
Registered
2025-07-18
Start date
2025-11-13
Completion date
Unknown
Last updated
2025-10-09

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

Conditions

Acute coronary syndrome and chronic coronary syndrome

Brief summary

Net Adverse Clinical Events (NACE), a composite of all-cause mortality, myocardial infarction, definite stent thrombosis, ischemic stroke, major bleeding or clinically relevant non-major bleeding defined as BARC type 2, 3 or 5

Detailed description

Treatment satisfaction, based on the Treatment Satisfaction Questionnaire for Medication II (TSQM-II), Treatment adherence, based on the Morisky Medication Adherence Scale (MMAS-8), Each individual component of the primary endpoint, Cardiovascular mortality, Non-cardiovascular mortality, Any need for revascularization, Major or clinically relevant non-major bleeding defined as BARC type 2, 3 or 5, Minor or clinically relevant non-major bleeding defined as BARC type 2 at 1, 6 and 12 month(s), Any periprocedural complications, On-treatment platelet reactivity at week 2 in the first 40 patients, Non-adherence to antiplatelet regimen

Interventions

Sponsors

Amsterdam UMC Stichting
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Net Adverse Clinical Events (NACE), a composite of all-cause mortality, myocardial infarction, definite stent thrombosis, ischemic stroke, major bleeding or clinically relevant non-major bleeding defined as BARC type 2, 3 or 5

Secondary

MeasureTime frame
Treatment satisfaction, based on the Treatment Satisfaction Questionnaire for Medication II (TSQM-II), Treatment adherence, based on the Morisky Medication Adherence Scale (MMAS-8), Each individual component of the primary endpoint, Cardiovascular mortality, Non-cardiovascular mortality, Any need for revascularization, Major or clinically relevant non-major bleeding defined as BARC type 2, 3 or 5, Minor or clinically relevant non-major bleeding defined as BARC type 2 at 1, 6 and 12 month(s), Any periprocedural complications, On-treatment platelet reactivity at week 2 in the first 40 patients, Non-adherence to antiplatelet regimen

Countries

Netherlands

Outcome results

None listed

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