Pediatric Intubation

NCT ID: NCT02289872

Last Updated: 2015-01-26

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

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-11-30

Study Completion Date

2014-12-31

Brief Summary

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The aim of the study was to compare time and success rates of TruView PCD video laryngoscope and Macintosh laryngoscope for the pediatric emergency intubation with three airway scenarios in a standardized manikin model.

Detailed Description

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Conditions

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Intubation 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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Scenario A

The control scenario, where neither chest compression nor cervical stabilization was applied during intubation.

Group Type EXPERIMENTAL

Macintosh Laryngoscope

Intervention Type DEVICE

Direct-Laryngoscopy

TruView PCD Video laryngoscope

Intervention Type DEVICE

Video-Laryngoscopy

Scenario B

The chest compression scenario, where continuous chest compression was applied using chest compression system LUCAS-2 (Physio-Control, Redmond, WA, USA). Chest compression was provided at a rate of 100 min-1 to a depth of 5-6 cm during all intubation procedures.

Group Type EXPERIMENTAL

Macintosh Laryngoscope

Intervention Type DEVICE

Direct-Laryngoscopy

TruView PCD Video laryngoscope

Intervention Type DEVICE

Video-Laryngoscopy

Scenario C

The chest compression with cervical stabilization scenario, where both chest compression using Lucas-2 and cervical stabilization were applied. A correctly fitting standard cervical immobilization collar (StifNeck Select, Laerdal, Stavanger, Norway) was applied to the manikin's neck to prevent movement of the cervical spine.

Group Type EXPERIMENTAL

Macintosh Laryngoscope

Intervention Type DEVICE

Direct-Laryngoscopy

TruView PCD Video laryngoscope

Intervention Type DEVICE

Video-Laryngoscopy

Interventions

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Macintosh Laryngoscope

Direct-Laryngoscopy

Intervention Type DEVICE

TruView PCD Video laryngoscope

Video-Laryngoscopy

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* give voluntary consent to participate in the study
* inexperienced in pediatric intubation paramedics

Exclusion Criteria

* not meet the above criteria
* participants who had performed intubation in pediatric humans prior the trial or had previously TruView experience
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

Locations

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International Institute of Rescue Research and Education

Warsaw, Masovie, Poland

Site Status

Countries

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Poland

References

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Szarpak L, Czyzewski L, Kurowski A, Truszewski Z. Comparison of the TruView PCD video laryngoscope and macintosh laryngoscope for pediatric tracheal intubation by novice paramedics: a randomized crossover simulation trial. Eur J Pediatr. 2015 Oct;174(10):1325-32. doi: 10.1007/s00431-015-2538-0. Epub 2015 Apr 18.

Reference Type DERIVED
PMID: 25894914 (View on PubMed)

Other Identifiers

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TruView/01

Identifier Type: -

Identifier Source: org_study_id

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