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Outcome of Longterm Antithrombotic Therapy in Acute Coronary Syndrome Patients

A Retrospective Epidemiological Study to Investigate Outcome and Mortality With Longterm Antithrombotic Therapy in Acute Coronary Syndrome Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01623700
Enrollment
78000
Registered
2012-06-20
Start date
2006-01-31
Completion date
Unknown
Last updated
2012-06-20

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

Conditions

Acute Coronary Syndrome, Myocardial Infarction

Keywords

clopidogrel, aspirin, percutaneous coronary intervention, coronary stenting, antiplatelet

Brief summary

This observational study will based on the Register of Information and Knowledge About Swedish Heart Intensive Care Admissions (RIKS-HIA) and the Swedish Coronary Angiography and Angioplasty Registry (SCAAR) which since 2009 are merged into The Swedish Web-system for Enhancement and Development of Evidence-based care in Heart disease Evaluated According to Recommended Therapies (SWEDEHEART). The aim of this study is to investigate the impact of different antithrombotic treatment options (treatment duration, type of treatment and combination of treatments) in Acute Coronary Syndrome (ACS) patients on outcomes such as recurrent ischemic events and mortality.

Interventions

None listed

Sponsors

AstraZeneca
CollaboratorINDUSTRY
Uppsala University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patient with an event of ACS under the study period * Patient found in the National Registry of Drug Prescriptions and treated or not treated with antithrombotic drug/s (acetylsalicylic acid and/or either clopidogrel/ticlopidine/prasugrel and/or warfarin)

Exclusion criteria

* Patients will not be excluded from the database if they fulfill inclusion criteria.

Design outcomes

Primary

MeasureTime frameDescription
number of patients with adverse events in patient groups with different antithrombotic treatment strategiesup to 5 years and 6 monthsadverse events such as: mortality, re-infarction, revascularization, ischemic- and non-ischemic stroke and bleeding

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026