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Identification of Ventricular Fibrillation and Optimization of Defibrillation During CPR

NCT02952105 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 90

Last updated 2016-11-02

No results posted yet for this study

Summary

It's so important to recognize ventricular fibrillation in cardiac arrest and defibrillation early. At the same time Research findings have identified high-quality CPR with minimum interruption is critical to the success of defibrillation therapy. Both the guidelines by American Heart Association and the guidelines by European Resuscitation Council emphasize the importance of minimizing interruptions in chest compressions, specifically, duration of the pre-shock and post-shock pauses. So AHA indicate that there will be a new algorithm of VF during chest compression, which has high sensitivity and specificity. And the investigators can identify VF and defibrillate earlier.

The aim of this study is to verify that if Sherlock algorithm of Philips MRx monitor/defibrillator can identify shockable rhythms during chest compression accurately.

Conditions

  • Cardiac Arrest
  • Identify of Electrocadiac Rhythm

Sponsors & Collaborators

  • Peking Union Medical College Hospital

    collaborator OTHER

  • Jinhua Central Hospital

    collaborator OTHER

  • The First Affiliated Hospital of Henan University of Science and Technology

    lead OTHER

Principal Investigators

  • Xuezhong Yu, Doctor · Peking Union Medical College Hospital

  • Guoxiu Zhang, Bachelor · The First Affiliated Hospital of Henan University of Science and Technology

  • Mingwei Huang, Bachelor · Jinhua Central Hospital

Eligibility

Min Age
14 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2017-10-31
Completion
2018-05-31

Countries

  • China

Study Locations

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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 NCT02952105 on ClinicalTrials.gov