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Long-term Follow-up of antithrombotIc Management Patterns in Acute Coronary Syndrome Patients in Asia-China Extension

EPICOR Asia-China Extension. Long-term Follow-up of antithrombotIc Management Patterns in Acute Coronary Syndrome Patients in Asia-China Extension

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02305680
Acronym
EPICOR
Enrollment
2334
Registered
2014-12-03
Start date
2014-12-17
Completion date
2017-04-05
Last updated
2018-09-17

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

Conditions

Acute Coronary Syndromes

Brief summary

This study is to describe the long-term antithrombotic management patterns in a real-life setting for patients hospitalized with an acute coronary syndrome in China.

Detailed description

This study is to describe the long-term (3 to 5 years after the acute coronary syndrome index event) antithrombotic management patterns in a real-life setting for patients hospitalized with an acute coronary syndrome (i.e. ST-segment Elevation Myocardial Infarction, Non-ST-segment Elevation Myocardial Infarction, Unstable Angina) in China.

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Written informed consent has been provided. 2. Contact Order Form has been provided 3. Aged 18 years or older. 4. Enrolled in EPICOR Asia study and completed the 2 year follow-up.

Exclusion criteria

1. Presence of any condition/circumstance which in the opinion of the investigator could significantly limit the complete follow up of the patient (e.g. tourist, non-native speaker or does not understand the local language, psychiatric disturbances, alcohol or drug abuse). 2. Already included in the EPICOR Asia-China Extension observational study. 3. Presence of serious/severe co-morbidities in the opinion of the investigator which may limit short term (i.e. 6 month) life expectancy. 4. Current participation in an interventional clinical trial. 5. Patients receiving ticagrelor beyond 12 months and other off label use.

Design outcomes

Primary

MeasureTime frame
Long-term antithrombotic management patterns in a real-life setting by assessing the medication and treatment prescribed by physiciansFrom 2 years after the acute coronary syndrome index event, assessed up to 5 years

Secondary

MeasureTime frame
Clinical outcomes by record the number and type of cardiovascular and non-cardiovascular eventsFrom 2 years after the acute coronary syndrome index event, assessed up to 5 years
Health care resource consumption and related costs by assessing the detail hospitalization and outpatient cost.From 2 years after the acute coronary syndrome index event, assessed up to 5 years
Quality of life by assessing EQ-5D questionnaire.2 years,2.5years,3years,3.5years,4years,4.5years,5years after the acute coronary syndrome index event

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026