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Long-tErm Follow-uP of antithrombotIc Management Patterns In Acute CORonary Syndrome Patients in Asia

Completed
Conditions
Acute Coronary Syndrome
Registration Number
NCT01361386
Lead Sponsor
AstraZeneca
Brief Summary

The purpose of this study is to describe the short-and long-tern (i.e. up to 2 years following the index event) AMPs in patients hospitalized for an acute coronary syndrome (i.e. STEMI or NSTE-ACS), and to document clinical outcomes, economic aspects and impact on quality of life of these AMPs in a 'real-life' setting.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
13011
Inclusion Criteria
  • Written informed consent has been provided.
  • Diagnosis of STEMI, NSTEMI or UA
  • Hospitalization for the first time within 48 hours of onset of symptoms.
Exclusion Criteria
  • UA, STEMI, NSTEMI precipitated by or as a complication of surgery, trauma, or GI bleeding or post-PCI UA, STEMI and NSTEMI occurring in patients already hospitalized for other reasons.
  • Current participation in a randomised interventional clinical trial.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
short- and long-term medication and treatment prescribed by physicians in real-life settingup to 3 years
Secondary Outcome Measures
NameTimeMethod
clinical outcome (Cardiovascular events)up to 3 years
quality of life (EQ-5D questionnaire)up to 3 years
cost of hospitalizationup to 3 years

Trial Locations

Locations (1)

Research Site

🇻🇳

Hue, Vietnam

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