Real World Assessment of Effects of Beta-blockers on Patients With Acute Coronary Syndrome
NCT ID: NCT03669991
Last Updated: 2018-09-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
2200 participants
OBSERVATIONAL
2018-08-31
2022-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patients diagnosed as acute coronary syndromes including acute ST-segment elevation myocardial infarction (STEMI) and non-ST-segment elevated acute coronary syndrome (NSTE-ACS)
* Patients or whose legal representatives signed written informed consent form
Exclusion Criteria
* Pregnant or lactating women
* Patients without signed written informed consent
* Patients who was considered by the researcher inappropriate to participate in this study (for example, patients with a higher risk of cardiogenic shock, etc.)
18 Years
120 Years
ALL
No
Sponsors
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Chinese Academy of Medical Sciences, Fuwai Hospital
OTHER
Responsible Party
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Yi-Da Tang
Professor
Principal Investigators
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Yi-Da Tang, MD
Role: PRINCIPAL_INVESTIGATOR
Chinese Academy of Medical Sciences, Fuwai Hospital
Locations
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Fuwai Hospital, Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Yi-Da Tang
Role: primary
Other Identifiers
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20181082
Identifier Type: -
Identifier Source: org_study_id
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