Role of Airtraq Mobile to Improve Intubation Conditions With Airtraq

NCT ID: NCT02510924

Last Updated: 2018-01-02

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

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-08-31

Study Completion Date

2017-11-05

Brief Summary

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Airtraq sp has been proven effective for intubating patients presenting with difficult airway.

The Airtraq sp allows visualisation of the tracheal inlet only for the intubator.

By adding a smartphone with a dedicated app (Airtraq Mobile) to the Airtraq sp, the visualisation of the tracheal inlet is possible for all the airway providers.

The investigators aim to demonstrate that the addition of the Airtraq Mobile app improves success rate of intubation (primary endpoint), as well as confort of the airway provider, shortens time for intubation and reduces injury to the patients.

Detailed Description

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Airtraq sp has been proven effective for intubating patients presenting with difficult airway.

The Airtraq sp allows visualisation of the tracheal inlet only for the intubator.

By adding a smartphone with a dedicated app (Airtraq Mobile) to the Airtraq sp, the visualisation of the tracheal inlet is possible for all the airway providers.

The investigators aim to demonstrate that the addition of the Airtraq Mobile app improves success rate of intubation (primary endpoint), as well as confort of the airway provider, shortens time for intubation and reduces injury to the patients while their neck is imobilized by a cervical collar, creating a simulated difficult airway.

Patients will be included if they necessitate an elective general anesthesia and orotracheal intubation.

Exclusion criteria are related to difficult airway, ASA IV and patient refusal.

Conditions

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Nasal Obstruction Arthrosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Tracheal intubation with Airtraq sp

Tracheal intubation with Airtraq sp.

Group Type ACTIVE_COMPARATOR

Tracheal intubation

Intervention Type DEVICE

tracheal intubation with Airtraq sp vs Airtraq mobile

Tracheal intubation with Airtraq Mobile

Tracheal intubation with Airtraq Mobile

Group Type EXPERIMENTAL

Tracheal intubation

Intervention Type DEVICE

tracheal intubation with Airtraq sp vs Airtraq mobile

Interventions

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Tracheal intubation

tracheal intubation with Airtraq sp vs Airtraq mobile

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* American Society of Anesthesia classification 1-3, elective surgey necessitating general anesthesia and intubation, patient consent

Exclusion Criteria

* American Society of Anesthesia classification 4, patient refusal, history of difficult airway
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Lausanne Hospitals

OTHER

Sponsor Role lead

Responsible Party

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Patrick Schoettker,MD PD

MD, PD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Patrick Schoettker, MD, PD

Role: PRINCIPAL_INVESTIGATOR

University of Lausanne Hospitals

Locations

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Dpt of Anesthesiology, University of Lausanne CHUV

Lausanne, Canton of Vaud, Switzerland

Site Status

Countries

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Switzerland

References

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Schoettker P, Corniche J. The AirView Study: Comparison of Intubation Conditions and Ease between the Airtraq-AirView and the King Vision. Biomed Res Int. 2015;2015:284142. doi: 10.1155/2015/284142. Epub 2015 Jun 16.

Reference Type BACKGROUND
PMID: 26161393 (View on PubMed)

Other Identifiers

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409/14

Identifier Type: -

Identifier Source: org_study_id

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