- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03286491
Clinical Decision Support System to Define 30 Day Adverse Clinical Events for Emergency Department Acute Coronary Syndromes
September 15, 2017 updated by: Serhat Akay, Turkish Ministry of Health Izmir Teaching Hospital
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
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.
Study Overview
Status
Unknown
Intervention / Treatment
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.
Study Type
Observational
Enrollment (Anticipated)
400
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nesli Belen, M.D.
- Phone Number: 90-551-4363001
- Email: neslibelen@yahoo.com
Study Contact Backup
- Name: Serhat Akay, M.D.
- Phone Number: 90-505-7079350
- Email: howls_Castle@mynet.com
Study Locations
-
-
-
Izmir, Turkey, 35000
- Recruiting
- Izmir Bozyaka Training and Research Hospital
-
Contact:
- Nesli Belen, M.D.
- Phone Number: 90-551-4363001
- Email: neslibelen@yahoo.com
-
Contact:
- Serhat Akay, M.D.
- Phone Number: 90-505-7079350
- Email: howls_Castle@mynet.com
-
-
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
Patients presenting to emergency deparmtent with acute chest pain consistent with acute coronary syndrome will be included for analysis.
Description
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
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 |
Intervention / Treatment |
---|---|
Patients presenting with acute coronary syndrome
Patients presenting to emergency department with acute coronary syndrome
|
Study patients will be reviewed whether they will have coronary interventions in 30 days
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Non fatal myocardial infarction, cardiac related death or coronary intervention in 30 days
Time Frame: 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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
August 12, 2017
Primary Completion (Anticipated)
December 12, 2017
Study Completion (Anticipated)
February 1, 2018
Study Registration Dates
First Submitted
September 15, 2017
First Submitted That Met QC Criteria
September 15, 2017
First Posted (Actual)
September 18, 2017
Study Record Updates
Last Update Posted (Actual)
September 18, 2017
Last Update Submitted That Met QC Criteria
September 15, 2017
Last Verified
September 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- TurkishMOHITH
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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