Vfib by ECG or Echo During Cardiac Arrest

NCT04906252 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 813

Last updated 2025-04-02

No results posted yet for this study

Summary

The goal of this study is to measure survival rates associated with patients presenting in cardiac arrest based on their electrocardiographic rhythm and their echocardiographic rhythm. Electrocardiographic rhythm is defined as the rhythm on the ECG and echocardiographic rhythm is the rhythm visualized on bedside ultrasound. Specifically, we will categorize patients based on identical rhythms and dichotomous rhythms with an interest in outcomes in the patient group where their echocardiographic and electrographic rhythms do not match. This is important as current ACLS protocols use electrocardiographic rhythms to determine therapy but limited research implies that therapeutic decisions based on echocardiographic rhythm may produce increased survival.

This study will occur during emergency department resuscitation of patients presenting in cardiac arrest. Patients presenting to the emergency department after cardiac arrest will undergo standard resuscitation based on ACLS protocols. Ultrasound imaging will be performed as soon as possible after the patient arrives and digitally recorded, as is currently the standard of care at the institute. Simultaneous recording of the ECG rhythm strip will occur as well. This will be repeated for as many pauses in CPR as is warranted.

Each site will record data based on the Utstein nomenclature including patient demographics, arrest details and survival outcomes. Ultrasound images and ECG recordings will be de-identified and submitted to a central database. Data will be uploaded into a centralized database. Statistical analysis will analyze outcomes based on echocardiographic and sonographic findings. Our aim is to measure the survival benefit of treating out of hospital cardiac arrest using echocardiographic rhythm instead of electrocardiographic rhythm.

Conditions

  • Cardiac Arrest

Interventions

DIAGNOSTIC_TEST

Echocardiography

Patients presenting in cardiac arrest will undergo echocardiography as is the standard of care at their institution

DIAGNOSTIC_TEST

Electrocardiogram (ECG)

Patients presenting in cardiac arrest will undergo an electrocardiogram (ECG) as is the standard of care at their institution

Sponsors & Collaborators

  • Temple University

    collaborator OTHER
  • Stony Brook University

    collaborator OTHER
  • University of Ottawa

    collaborator OTHER
  • ChristianaCare

    collaborator OTHER
  • Boston Medical Center

    collaborator OTHER
  • Dartmouth College

    collaborator OTHER
  • University of Alabama at Birmingham

    collaborator OTHER
  • University of Rochester

    collaborator OTHER
  • Baystate Medical Center

    collaborator OTHER
  • Medical College of Wisconsin

    collaborator OTHER
  • University of Pennsylvania

    collaborator OTHER
  • Prisma Health-Midlands

    collaborator OTHER
  • Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)

    collaborator OTHER
  • Staten Island University Hospital

    collaborator OTHER
  • State University of New York - Upstate Medical University

    collaborator OTHER
  • University of Manitoba

    collaborator OTHER
  • Mayo Clinic

    collaborator OTHER
  • Kaweah Delta Health Care District

    collaborator OTHER
  • SBH Health System

    collaborator OTHER
  • Yale University

    collaborator OTHER
  • Johns Hopkins University

    collaborator OTHER
  • The University of Texas at San Antonio

    collaborator OTHER
  • Wake Forest University Health Sciences

    collaborator OTHER
  • University of Arkansas

    collaborator OTHER
  • Valleywise Health

    collaborator OTHER
  • Kendall Healthcare Group, Ltd.

    collaborator INDUSTRY
  • Truman Medical Center

    collaborator OTHER
  • Oregon Health and Science University

    collaborator OTHER
  • Vassar Brothers Medical Center

    collaborator OTHER
  • Brookdale University Hospital Medical Center

    collaborator OTHER
  • University of Kansas Medical Center

    collaborator OTHER
  • University of Maine

    collaborator OTHER
  • University of Colorado, Denver

    collaborator OTHER
  • Duke University

    collaborator OTHER
  • University at Buffalo

    collaborator OTHER
  • North Shore University Hospital

    collaborator OTHER
  • Hartford Hospital

    collaborator OTHER
  • Louisiana State University Health Sciences Center in New Orleans

    collaborator OTHER
  • University of Florida

    collaborator OTHER
  • University of Maryland

    collaborator OTHER
  • Sutter Medical Foundation

    collaborator OTHER
  • Arizona School of Health Sciences

    collaborator OTHER
  • Virginia Commonwealth University

    collaborator OTHER
  • Romolo Gaspari

    lead OTHER

Principal Investigators

  • Romolo Gaspari, MD, PhD · UMass Medical School

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-15
Primary Completion
2024-12-31
Completion
2025-01-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04906252 on ClinicalTrials.gov