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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02510924
Other study ID # 409/14
Secondary ID
Status Completed
Phase N/A
First received July 27, 2015
Last updated December 29, 2017
Start date August 2015
Est. completion date November 5, 2017

Study information

Verified date December 2017
Source University of Lausanne Hospitals
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date November 5, 2017
Est. primary completion date November 5, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Tracheal intubation
tracheal intubation with Airtraq sp vs Airtraq mobile

Locations

Country Name City State
Switzerland Dpt of Anesthesiology, University of Lausanne CHUV Lausanne VD

Sponsors (1)

Lead Sponsor Collaborator
University of Lausanne Hospitals

Country where clinical trial is conducted

Switzerland, 

References & Publications (1)

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. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Success Success of intubation within time frame 180 seconds
Secondary Number of attempts Success of intubation within time frame 180 seconds
Secondary Number of injuries Injuries within time frame 180 seconds
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