- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01361386
Long-tErm Follow-uP of antithrombotIc Management Patterns In Acute CORonary Syndrome Patients in Asia (EPICOR ASIA)
June 13, 2014 updated by: AstraZeneca
Long-Term Follow-up of Antithrombotic Management Patterns in Acute Coronary Syndrome Patients in Asia
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.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
13011
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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HongKong, China
- Research Site
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Ningxia, China
- Research Site
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Qingdao, China
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Anhui
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Hefei, Anhui, China
- Research Site
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Wuhu, Anhui, China
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Beijing
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Beijing, Beijing, China
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Chongqing
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Chongqing, Chongqing, China
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Fujian
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Fuzhou, Fujian, China
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Gansu
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Lanzhou, Gansu, China
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Guangdong
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Foshan, Guangdong, China
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Guangzhou, Guangdong, China
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Shenzhen, Guangdong, China
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Guangxi
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Nanning, Guangxi, China
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Yulin, Guangxi, China
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Guizhou
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Guiyang, Guizhou, China
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Hebei
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Baoding, Hebei, China
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Shijiazhuang, Hebei, China
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Tangshan, Hebei, China
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Heilongjiang
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Daqing, Heilongjiang, China
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Harbin, Heilongjiang, China
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Henan
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Zhengzhou, Henan, China
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Hubei
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Shiyan, Hubei, China
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Wuhan, Hubei, China
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Hunan
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Changsha, Hunan, China
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Jiangsu
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Nanjing, Jiangsu, China
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Wuxi, Jiangsu, China
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Xuzhou, Jiangsu, China
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Zhenjiang, Jiangsu, China
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Jilin
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Changchun, Jilin, China
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Liaoning
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Jinzhou, Liaoning, China
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Shenyang, Liaoning, China
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Yingkou, Liaoning, China
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Qinghai
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Xining, Qinghai, China
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Shaanxi
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Xi'an, Shaanxi, China
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Shandong
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Jinan, Shandong, China
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Shanghai
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Shanghai, Shanghai, China
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Shanxi
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Changzhi, Shanxi, China
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Jinzhong, Shanxi, China
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Taiyuan, Shanxi, China
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Sichuan
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Chengdu, Sichuan, China
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Tianjin
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Tianjin, Tianjin, China
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Xinjiang
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Shihezi, Xinjiang, China
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Urumuqi, Xinjiang, China
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Yunnan
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Kunming, Yunnan, China
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Zhejiang
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Hangzhou, Zhejiang, China
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Delhi, India
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Andhra Pradesh
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Hyderabad, Andhra Pradesh, India
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Assam
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Guwahati, Assam, India
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Gujarat
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Ahmedabad, Gujarat, India
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Baroda, Gujarat, India
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Surat, Gujarat, India
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Haryana
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Gurgaon, Haryana, India
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Karnataka
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Bangalore, Karnataka, India
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Manipal, Karnataka, India
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Kerala
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Kochi, Kerala, India
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Trivandrum, Kerala, India
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Madhya Pradesh
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Bhopal, Madhya Pradesh, India
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Bilaspur, Madhya Pradesh, India
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Maharashtra
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Aurangabad, Maharashtra, India
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Mumbai, Maharashtra, India
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Nagpur, Maharashtra, India
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Pune, Maharashtra, India
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Punjab
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Ludhiana, Punjab, India
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Mohali, Punjab, India
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Rajasthan
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Ajmer, Rajasthan, India
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Jaipur, Rajasthan, India
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Tamil Nadu
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Chennai, Tamil Nadu, India
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Coimbatore, Tamil Nadu, India
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Madurai, Tamil Nadu, India
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Uttar Pradesh
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Lucknow, Uttar Pradesh, India
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West Bengal
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Kolkata, West Bengal, India
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Busan, Korea, Republic of
- Research Site
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Chuncheon, Korea, Republic of
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Deagu, Korea, Republic of
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Gwangju, Korea, Republic of
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Jeju, Korea, Republic of
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Pusan, Korea, Republic of
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Seoul, Korea, Republic of
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Chungcheongnam-do
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Cheonan, Chungcheongnam-do, Korea, Republic of
- Research Site
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Gyeonggi-do
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Bucheon, Gyeonggi-do, Korea, Republic of
- Research Site
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Goyang-si, Gyeonggi-do, Korea, Republic of
- Research Site
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Suwon, Gyeonggi-do, Korea, Republic of
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Gyeongsangnamdo
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Yangsan, Gyeongsangnamdo, Korea, Republic of
- Research Site
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Jeollabuk-do
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IKsan, Jeollabuk-do, Korea, Republic of
- Research Site
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Penang, Malaysia
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Kuching
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Sarawak, Kuching, Malaysia
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Singapore, Singapore
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Bangkok
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Bangkoknoi, Bangkok, Thailand
- Research Site
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Huaykwang, Bangkok, Thailand
- Research Site
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PathumWan, Bangkok, Thailand
- Research Site
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Payathai, Bangkok, Thailand
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Rachathevi, Bangkok, Thailand
- Research Site
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Saimai, Bangkok, Thailand
- Research Site
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Chanthaburi
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Muang, Chanthaburi, Thailand
- Research Site
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Chiangmai
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Muang, Chiangmai, Thailand
- Research Site
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Chiangrai
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Muang, Chiangrai, Thailand
- Research Site
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Chonburi
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Muang, Chonburi, Thailand
- Research Site
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Khonkaen
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Muang, Khonkaen, Thailand
- Research Site
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Lampang
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Muang, Lampang, Thailand
- Research Site
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Nakornratchaseema
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Muang, Nakornratchaseema, Thailand
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Nan
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Muang, Nan, Thailand
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Pathumthani
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Klongluang, Pathumthani, Thailand
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Phitsanulok
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Muang, Phitsanulok, Thailand
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Songkla
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Muang, Songkla, Thailand
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Suphanburi
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Muang, Suphanburi, Thailand
- Research Site
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Surat Thani
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Muang, Surat Thani, Thailand
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Udonthani
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Muang, Udonthani, Thailand
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Ho Chi Minh City, Vietnam
- Research Site
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Hue, Vietnam
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Asian patients hospitalized for ACS within 48 hours of symptom onset and who have a final diagnosis of unstable angina (UA), STEMI or non-ST-segment elevation myocardial infarction (NSTEMI).
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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1
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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short- and long-term medication and treatment prescribed by physicians in real-life setting
Time Frame: up to 3 years
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up to 3 years
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
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clinical outcome (Cardiovascular events)
Time Frame: up to 3 years
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up to 3 years
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cost of hospitalization
Time Frame: up to 3 years
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up to 3 years
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quality of life (EQ-5D questionnaire)
Time Frame: up to 3 years
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up to 3 years
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Guy Yeoman, AstraZeneca
- Study Chair: Prof. Huo Yong, Peking University 1st Hospital
- Study Chair: Jayanti Visvanathan, AstraZeneca
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Huo Y, Van de Werf F, Han Y, Rossello X, Pocock SJ, Chin CT, Lee SW, Li Y, Jiang J, Vega AM, Medina J, Bueno H. Long-Term Antithrombotic Therapy and Clinical Outcomes in Patients with Acute Coronary Syndrome and Renal Impairment: Insights from EPICOR and EPICOR Asia. Am J Cardiovasc Drugs. 2021 Jul;21(4):471-482. doi: 10.1007/s40256-020-00447-5. Epub 2021 Feb 4.
- Guan S, Xu X, Li Y, Li J, Guan M, Wang X, Jing Q, Huo Y, Han Y. Impact of Diabetes Mellitus on Antithrombotic Management Patterns and Long-Term Clinical Outcomes in Patients With Acute Coronary Syndrome: Insights From the EPICOR Asia Study. J Am Heart Assoc. 2020 Nov 17;9(22):e013476. doi: 10.1161/JAHA.119.013476. Epub 2020 Nov 7.
- Zhang S, Wang W, Sawhney JPS, Krittayaphong R, Kim HS, Nhan VT, Lee SW, Ong TK, Chin CT, Pocock SJ, Huo Y, Qian J, Ge J. Antithrombotic management and long-term outcomes following percutaneous coronary intervention for acute coronary syndrome in Asia. Int J Cardiol. 2020 Jul 1;310:16-22. doi: 10.1016/j.ijcard.2020.01.008. Epub 2020 Mar 17.
- Jan S, Lee SW, Sawhney JPS, Ong TK, Chin CT, Kim HS, Krittayaphong R, Nhan VT, Pocock SJ, Vega AM, Hayashi N, Huo Y. Predictors of high-cost hospitalization in the treatment of acute coronary syndrome in Asia: findings from EPICOR Asia. BMC Cardiovasc Disord. 2018 Jul 4;18(1):139. doi: 10.1186/s12872-018-0859-4.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2011
Primary Completion (Actual)
May 1, 2014
Study Completion (Actual)
May 1, 2014
Study Registration Dates
First Submitted
May 23, 2011
First Submitted That Met QC Criteria
May 25, 2011
First Posted (Estimate)
May 26, 2011
Study Record Updates
Last Update Posted (Estimate)
June 16, 2014
Last Update Submitted That Met QC Criteria
June 13, 2014
Last Verified
June 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NIS-CAP-XXX-2011/1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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