Intubation During Pediatric Resuscitation

NCT ID: NCT02277015

Last Updated: 2014-11-13

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

94 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-10-31

Study Completion Date

2014-11-30

Brief Summary

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The European Resuscitation Council (ERC) 2010 cardiopulmonary resuscitation (CPR) guidelines suggest that intubators should be able to secure the airway without interrupting chest compression. We examine the performance of the Berci-Kaplan DCI (BERCI), the GlideScope (GVL), the AirTraq, the Pentax AWS (Pentax) and the Miller laryngoscope (MIL) for endotracheal intubation (ETI) during pediatric resuscitation with and without chest compressions.

Detailed Description

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Conditions

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Cardiac Arrest Endotracheal Intubation Pediatric Manikin

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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ETI without chest compressions

Endotracheal intubation during pediatric resuscitation without chest compressions.

Group Type EXPERIMENTAL

Miller Laryngoscope

Intervention Type DEVICE

Direct Laryngoscopy

The Berci-Kaplan DCI

Intervention Type DEVICE

Videolaryngoscope-1

The AirTraq

Intervention Type DEVICE

Videolaryngoscope-2

GlideScope GVL

Intervention Type DEVICE

Videolaryngoscope-3

The Pentax AWS

Intervention Type DEVICE

Videolaryngoscope-4

ETI with chest compressions

Endotracheal intubation during pediatric resuscitation with chest compressions. Chest compression was performed using LUCAS-2 (Physio-Control).

Group Type EXPERIMENTAL

Miller Laryngoscope

Intervention Type DEVICE

Direct Laryngoscopy

The Berci-Kaplan DCI

Intervention Type DEVICE

Videolaryngoscope-1

The AirTraq

Intervention Type DEVICE

Videolaryngoscope-2

GlideScope GVL

Intervention Type DEVICE

Videolaryngoscope-3

The Pentax AWS

Intervention Type DEVICE

Videolaryngoscope-4

Interventions

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Miller Laryngoscope

Direct Laryngoscopy

Intervention Type DEVICE

The Berci-Kaplan DCI

Videolaryngoscope-1

Intervention Type DEVICE

The AirTraq

Videolaryngoscope-2

Intervention Type DEVICE

GlideScope GVL

Videolaryngoscope-3

Intervention Type DEVICE

The Pentax AWS

Videolaryngoscope-4

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* give voluntary consent to participate in the study
* minimum 1 year of work experience in emergency medicine
* experienced emergency medicine personnel (physicians, nurses, paramedics)

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

National Institute of Cardiology, Warsaw, Poland

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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ETI/2014/02

Identifier Type: -

Identifier Source: org_study_id