Pediatric Intubation During Resuscitation

NCT ID: NCT02277405

Last Updated: 2014-10-29

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

150 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 the study was to compare time and success rates of four intubation devices in a cardiopulmonary scenario with and without chest compressions with a standardized pediatric manikin model.

Detailed Description

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Emergency airway management during resuscitation is a critical skill in emergency medicine. According to the European Resuscitation Council (ERC) guidelines for resuscitation 2010 , endotracheal intubation (ETI) is considered the gold standard during resuscitation.

Conditions

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Intubation Resuscitation

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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Intubation without chest compressions

Endotracheal intubation of pediatric mannikin during resuscitation without chest compressions.

Group Type EXPERIMENTAL

Shikani Optical Stylet

Intervention Type DEVICE

Optical intubation

Endoeye Flexible Intubation (LF-V)

Intervention Type DEVICE

endoscopy intubation

Intubation with uninterrupted chest compressions

Endotracheal intubation of pediatric mannikin during resuscitation with uninterrupted chest compressions. In order to simulate the difficulties associated with intubation during uninterrupted chest compressions, CPR was performed by using LUCAS-2 (Physio-Control, Redmond, WA, U.S.).

Group Type EXPERIMENTAL

Shikani Optical Stylet

Intervention Type DEVICE

Optical intubation

Endoeye Flexible Intubation (LF-V)

Intervention Type DEVICE

endoscopy intubation

Interventions

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Shikani Optical Stylet

Optical intubation

Intervention Type DEVICE

Endoeye Flexible Intubation (LF-V)

endoscopy intubation

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 medical personnel (paramedics, nurses, 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

National Institute of Cardiology, Warsaw, Poland

Locations

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International Institute of Rescue Research and Education

Warsaw, Masovia, Poland

Site Status RECRUITING

Countries

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Poland

Central Contacts

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Lukasz Czyzewski

Role: CONTACT

+48696457655

Facility Contacts

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Lukasz Szarpak

Role: primary

(+48)500186225

Other Identifiers

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ETI/2014/04

Identifier Type: -

Identifier Source: org_study_id

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