Clinical Decision Support System to Define 30 Day Adverse Clinical Events for Emergency Department Acute Coronary Syndromes
NCT ID: NCT03286491
Last Updated: 2017-09-18
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
400 participants
OBSERVATIONAL
2017-08-12
2018-02-01
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
Study Groups
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Patients presenting with acute coronary syndrome
Patients presenting to emergency department with acute coronary syndrome
Further cardiac imaging
Study patients will be reviewed whether they will have coronary interventions in 30 days
Interventions
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Further cardiac imaging
Study patients will be reviewed whether they will have coronary interventions in 30 days
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients presenting with ST-segment elevation myocardial infarction
* Patients presenting with other causes of acute chest pain (pneumothorax, pulmonary -embolism, aortic dissection
* Decline to participate in study
18 Years
ALL
No
Sponsors
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Turkish Ministry of Health Izmir Teaching Hospital
OTHER_GOV
Responsible Party
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Serhat Akay
M.D.
Locations
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Izmir Bozyaka Training and Research Hospital
Izmir, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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TurkishMOHITH
Identifier Type: -
Identifier Source: org_study_id