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Pediatric Difficult Intubation

NCT ID: NCT02295670

Last Updated: 2014-11-20

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

180 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-11-30

Study Completion Date

2014-12-31

Brief Summary

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Endotracheal intubation (ETI) is perceived as the optimal method of providing and maintaining a clear and secure airway. The 2010 European Resuscitation Council (ERC) guidelines emphasized the importance of minimal interruption during cardiopulmonary resuscitation (CPR). These guidelines also suggest that skilled operators should be able to secure the airway without interrupting chest compression. The aim of the study was to compare time and success rates of the Vividtrac video-laryngoscope and the Miller laryngoscope for emergency intubation during simulated pediatric CPR.

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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Endotracheal intubation without chest compressions

Endotracheal intubation of mannikin during resuscitation without chest compressions.

Group Type EXPERIMENTAL

Vividtrac

Intervention Type DEVICE

video-laryngoscopy

MIL

Intervention Type DEVICE

direct-laryngoscopy

Endotracheal intubation with uninterrupted chest compressions

Endotracheal intubation of 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

Vividtrac

Intervention Type DEVICE

video-laryngoscopy

MIL

Intervention Type DEVICE

direct-laryngoscopy

Interventions

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Vividtrac

video-laryngoscopy

Intervention Type DEVICE

MIL

direct-laryngoscopy

Intervention Type DEVICE

Other Intervention Names

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miller larygoscopy

Eligibility Criteria

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Inclusion Criteria

* Give voluntary consent to participate in the study
* Paramedic student

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

Locations

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International Institute of Rescue Research and Education

Warsaw, Masovie, Poland

Site Status RECRUITING

Countries

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Poland

Central Contacts

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Lukasz Szarpak

Role: CONTACT

[email protected]
+48500186225

Facility Contacts

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Lukasz Szarpak

Role: primary

[email protected]
+48500186225

Other Identifiers

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ETI/2014/51

Identifier Type: -

Identifier Source: org_study_id