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Clinical Decision Support System to Define 30 Day Adverse Clinical Events for Emergency Department Acute Coronary Syndromes

Development of Clinical Decision Support System to Define 30 Day Adverse Clinical Events (Non Fatal Myocardial Infarction, Cardiac Related Death or Coronary Intervention) for Patients Presenting to Emergency Department With Acute Coronary Syndrome

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03286491
Enrollment
400
Registered
2017-09-18
Start date
2017-08-12
Completion date
2018-02-01
Last updated
2017-09-18

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

Conditions

Acute Coronary Syndrome, Clinical Decision Support System

Keywords

acute coronary syndrome, risk classification, 30 day adverse event, clinical decision support system

Brief summary

Acute coronary syndromes are among main complains for patients presenting to emergency department. Risk classification systems are used to classify patients to appropriate risks and help physicians manage diagnosis strategies and treatments. Purpose of this study is to develop a clinical decision support system for patients presenting to emergency department with the help of statistical machine learning.

Detailed description

Acute coronary syndromes are among main complains for patients presenting to emergency department and create a burden to emergency departments and hospitals. Risk classification systems were developed and used to classify patients to appropriate risk groups. According to risk classification, different diagnosis and treatment modalities can be used and help physicians manage diagnosis strategies and treatments. Purpose of this study is to develop a clinical decision support system for patients presenting to emergency department with the help of statistical machine learning.

Interventions

DIAGNOSTIC_TESTFurther cardiac imaging

Study patients will be reviewed whether they will have coronary interventions in 30 days

Sponsors

Turkish Ministry of Health Izmir Teaching Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Presenting to emergency department with acute chest pain consistent with acute coronary syndrome

Exclusion criteria

* Patients with less than 18 years old * 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

Design outcomes

Primary

MeasureTime frameDescription
Non fatal myocardial infarction, cardiac related death or coronary intervention in 30 days30 daysPatients will be screened for 30 days for Non fatal myocardial infarction, cardiac related death or coronary intervention (coronary angiogram, coronary artery bypass surgery)

Countries

Turkey (Türkiye)

Contacts

Primary ContactNesli Belen, M.D.
neslibelen@yahoo.com90-551-4363001
Backup ContactSerhat Akay, M.D.
howls_Castle@mynet.com90-505-7079350

Outcome results

None listed

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