REASON 1 Trial: Sonography in Cardiac Arrest

NCT01446471 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 793

Last updated 2015-12-02

No results posted yet for this study

Summary

The aim of this study is to investigate the predictive value of the presence or absence of cardiac activity by bedside ultrasound during cardiac arrest. The investigators anticipate based on previous research that patients who suffer a cardiac arrest and have cardiac activity on bedside ultrasound will have a greater chance of surviving to hospital admission. The investigators hypothesis is that the mortality rate in patients in cardiac arrest with no cardiac activity by ultrasound will have a mortality rate of 100%.

Conditions

  • Cardiac Arrest
  • Pulseless Electrical Activity
  • Asystole

Sponsors & Collaborators

  • North Shore University Hospital

    collaborator OTHER
  • NYU Langone Health

    collaborator OTHER
  • Mount Sinai Hospital, New York

    collaborator OTHER
  • Washington University School of Medicine

    collaborator OTHER
  • University of New Mexico

    collaborator OTHER
  • Wake Forest University Health Sciences

    collaborator OTHER
  • University of California, Irvine

    collaborator OTHER
  • University of Utah

    collaborator OTHER
  • Carolinas Medical Center

    collaborator OTHER
  • Emory University

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

    collaborator OTHER
  • Duke University

    collaborator OTHER
  • Brigham and Women's Hospital

    collaborator OTHER
  • Massachusetts General Hospital

    collaborator OTHER
  • Rhode Island Hospital

    collaborator OTHER
  • Christiana Care Health Services

    collaborator OTHER
  • George Washington University

    collaborator OTHER
  • Kingston Health Sciences Centre

    collaborator OTHER
  • University of Ottawa

    collaborator OTHER
  • Jewish General Hospital

    collaborator OTHER
  • Horizon Health Network

    collaborator OTHER
  • York Hospitals

    collaborator OTHER
  • Boston Medical Center

    collaborator OTHER
  • Indiana University

    collaborator OTHER
  • Yale University

    collaborator OTHER
  • Queen's Medical Center

    collaborator OTHER
  • University of Hawaii

    collaborator OTHER
  • Stanford University

    collaborator OTHER
  • University of Massachusetts, Worcester

    lead OTHER

Principal Investigators

  • Romolo Gaspari, MD, PhD · UMass Memorial Health

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2014-11-30
Completion
2015-11-30

Countries

  • United States
  • Canada

Study Locations

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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 NCT01446471 on ClinicalTrials.gov