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Clinical Trials/NCT02959788
NCT02959788
Completed
Not Applicable

Heart Rate Variability as a Predictor of Ischemic Heart Disease

University of Iowa1 site in 1 country62 target enrollmentApril 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Coronary Syndrome
Sponsor
University of Iowa
Enrollment
62
Locations
1
Primary Endpoint
Major adverse cardiac events
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Identification of patients who are at highest risk for heart attack is an important task for emergency medicine physicians. Currently, physicians use a variety of different scoring systems to stratify their risk for having a heart attack. Heart rate variability (HRV) is a measure derived from noninvasive cardiac monitoring. This data is collected from a simple, non-invasive chest strap during a 10-minute recording session. The purpose of this proposal is to collect heart rate variability data on patients admitted to the emergency department with chest pain. The intent is to measure the association between heart rate variability and the various risk stratification scoring systems for chest pain.

Detailed Description

Identification of patients who are at highest risk for heart attack is an important task for emergency medicine physicians. Currently, physicians use a variety of different scoring systems to stratify their risk for having a heart attack. Heart rate variability (HRV) is a measure derived from noninvasive cardiac monitoring. This data is collected from a simple, non-invasive chest strap during a 10-minute recording session. The purpose of this proposal is to collect heart rate variability data on patients admitted to the emergency department with chest pain. The intent is to measure the association between heart rate variability and the various risk stratification scoring systems for chest pain. The investigators propose to enroll patients admitted to the emergency department with chest pain. In addition to HRV data, clinical risk factors will be obtained, using validated clinical risk scoring systems. The team will follow patient's clinical course in order to include information about the determined cause of chest pain. The goal is to understand how HRV can augment common risk stratification scoring systems for patient presenting to the ED with chest pain.

Registry
clinicaltrials.gov
Start Date
April 2016
End Date
August 2016
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mohr, Nicholas M

Associate Professor

University of Iowa

Eligibility Criteria

Inclusion Criteria

  • Chest pain in ED

Exclusion Criteria

  • Prisoners
  • Pregnant women
  • Unable to consent

Outcomes

Primary Outcomes

Major adverse cardiac events

Time Frame: 30 days

Secondary Outcomes

  • HEART score(1 day)
  • Coronary heart disease risk factors(1 day)

Study Sites (1)

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