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

Acute Coronary Syndrome Clinical Trial

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03286491
• Other study ID #: TurkishMOHITH
• Status: Recruiting
• Phase: N/A
• First received: September 15, 2017
• Last updated: September 15, 2017
• Start date: August 12, 2017
• Est. completion date: February 1, 2018

Study information

• Verified date: September 2017
• Source: Turkish Ministry of Health Izmir Teaching Hospital
• Contact: Nesli Belen, M.D.
• Phone: 90-551-4363001
• Email: neslibelen[@]yahoo.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 400
• Est. completion date: February 1, 2018
• Est. primary completion date: December 12, 2017
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Acute Coronary Syndrome
• Clinical Decision Support System
• Emergencies
• Syndrome

Intervention

Diagnostic Test:
• Further cardiac imaging
Study patients will be reviewed whether they will have coronary interventions in 30 days

Locations

Country	Name	City	State
Turkey	Izmir Bozyaka Training and Research Hospital	Izmir

Sponsors (1)

Lead Sponsor	Collaborator
Turkish Ministry of Health Izmir Teaching Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Non fatal myocardial infarction, cardiac related death or coronary intervention in 30 days	Patients will be screened for 30 days for Non fatal myocardial infarction, cardiac related death or coronary intervention (coronary angiogram, coronary artery bypass surgery)	30 days