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

NCT ID: NCT02305680

Last Updated: 2018-09-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

2334 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-12-17

Study Completion Date

2017-04-05

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Acute Coronary Syndromes

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Yong Huo, Doctor

Role: PRINCIPAL_INVESTIGATOR

Peking University First Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Research Site

Baoding, , China

Site Status

Research Site

Beijing, , China

Site Status

Research Site

Changzhi, , China

Site Status

Research Site

Chongqing, , China

Site Status

Research Site

Guangzhou, , China

Site Status

Research Site

Guiyang, , China

Site Status

Research Site

Haerbin, , China

Site Status

Research Site

Hangzhou, , China

Site Status

Research Site

Hebei, , China

Site Status

Research Site

Jilin, , China

Site Status

Research Site

Jinan, , China

Site Status

Research Site

Jinzhong, , China

Site Status

Research Site

Kunming, , China

Site Status

Research Site

Lanzhou, , China

Site Status

Research Site

Nanjing, , China

Site Status

Research Site

Nanning, , China

Site Status

Research Site

Shanghai, , China

Site Status

Research Site

Shenyang, , China

Site Status

Research Site

Shenzhen, , China

Site Status

Research Site

Shihezi, , China

Site Status

Research Site

Taiyuan, , China

Site Status

Research Site

Tangshan, , China

Site Status

Research Site

Tianjin, , China

Site Status

Research Site

Ürümqi, , China

Site Status

Research Site

Wuhan, , China

Site Status

Research Site

Wuxi, , China

Site Status

Research Site

Xi'an, , China

Site Status

Research Site

Xining, , China

Site Status

Research Site

Xuzhou, , China

Site Status

Research Site

Yinchuan, , China

Site Status

Research Site

Yulin, , China

Site Status

Research Site

Zhengzhou, , China

Site Status

Research Site

Zhenjiang, , China

Site Status

Countries

Review the countries where the study has at least one active or historical site.

China

Related Links

Access external resources that provide additional context or updates about the study.

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

NIS-CCN-XXX-2014/1

Identifier Type: OTHER

Identifier Source: secondary_id

D1843R00049

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.