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NCT03887897

First Attempt Intubation Rate With Airtraq vs Macintosh Direct Laryngoscope

A Randomized Controlled Trial to Compare the First-pass Intubation Success of the Airtraq Laryngoscope Versus the Macintosh Direct Laryngoscope in Patients Requiring General Anaesthesia for Elective Operation.
Chinese University of Hong Kong·ClinicalTrials.gov·procedureRecruiting
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Study focus
Disease/Condition
Intubation
Drug/Device/Intervention
Tracheal Intubation
Study type
Interventional
Intervention type
procedure
Sponsor & location
Primary sponsor
Chinese University of Hong Kong
Location
Hong Kong, China
Timeline & enrollment
Phase
N/A
Start date
Oct 02, 2019
End date
Dec 01, 2022
Enrollment
1586 participants
Primary outcome

First-pass success in tracheal intubation

Summary

In recent decades, numerous videolaryngoscopes have been introduced to facilitate tracheal
 intubation. However, it remains unclear whether videolaryngoscope will increase the
 successful tracheal intubation compared with usual Macintosch laryngoscope. Therefore, this
 pilot study is a randomized controlled trial designed to compare the first-pass intubation
 success of the Airtraq laryngoscope versus the Macintosh direct laryngoscope in patients
 requiring general anesthesia for elective operation, with the aims to examine the feasibility
 of a large multicentre effectiveness trial by assessing recruitment targets, testing the data
 completeness, and local incidence of first-pass intubation success.

ICD-10 classifications
Failed or difficult intubationFailed or difficult intubation during labour and deliveryFailed or difficult intubation during pregnancyFailed or difficult intubation during the puerperiumRespiratory arrest
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT03887897
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT03887897 through Pure Global AI's free database. This phase not specified trial is sponsored by Chinese University of Hong Kong and is currently Recruiting. The study focuses on Intubation. Target enrollment is 1586 participants.

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