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Pediatric Resuscitation With Feedback CPR Devices

NCT ID: NCT02281903

Last Updated: 2014-11-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

132 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-10-31

Study Completion Date

2014-11-30

Brief Summary

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The aim of this study was to compare the TrueCPR feedback device (with metronome) to standard basic life support (BLS) in terms of the quality of single rescuer pediatric resuscitation. Therefore, our hypothesis was that there would be no difference between both CPR methods in terms of chest compression quality parameters.

Detailed Description

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Cardiac arrest is a leading cause of death worldwide. High-quality chest compressions are of paramount importance for survival and good neurological outcome. Unfortunately, even health professionals have difficulty performing effective CPR. Chest compression (CC) is often too shallow, compression ratio is inadequate, and hands-off time is too long. CPR feedback devices might be an option for rescuers to in order to increase CC efficiency.

Conditions

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Cardiac Arrest

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Chest compression of manikins chest

Compression of pediatric manikins chest according European Resuscitation Council 2010 guidelines for cardiopulmonary resuscitation.

Group Type EXPERIMENTAL

The TrueCPR feedback device

Intervention Type DEVICE

feedback devices

Standard BLS

Intervention Type DEVICE

Standard basic life support = chest compressions without any feedback device (manual resuscitation)

Interventions

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The TrueCPR feedback device

feedback devices

Intervention Type DEVICE

Standard BLS

Standard basic life support = chest compressions without any feedback device (manual resuscitation)

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* give voluntary consent to participate in the study
* medical profession (paramedics, nurses, physicians) or medical students (nurses, paramedics, physicians)

Exclusion Criteria

* not meet the above criteria
* wrist or low back diseases
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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International Institute of Rescue Research and Education

OTHER

Sponsor Role lead

Responsible Party

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Lukasz Szarpak

Lukasz Szarpak

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Lukasz Szarpak

Role: PRINCIPAL_INVESTIGATOR

Institute of Cardiology

Locations

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International Institute of Rescue Research and Education

Warsaw, Masovia, Poland

Site Status

Countries

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Poland

Other Identifiers

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CPR/2014/05

Identifier Type: -

Identifier Source: org_study_id