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Comparison of Two Videolaryngoscopes (C-MAC vs Airtraq) for Awake Intubation - Trial NCT05428995

Access comprehensive clinical trial information for NCT05428995 through Pure Global AI's free database. This phase not specified trial is sponsored by Hospital Clinico Universitario de Santiago and is currently Recruiting. The study focuses on Intubation. Target enrollment is 90 participants.

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Trial Details
ClinicalTrials.gov โ€ข NCT05428995
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Comparison of Two Videolaryngoscopes (C-MAC vs Airtraq) for Awake Intubation
A Randomized Comparison Between the C-MAC and Airtraq Videolaryngoscopes for First-attempt Intubation Success in Awake Patients With Anticipated Difficult Airway.

Study Focus

Intubation

C-MAC videolaryngoscope

Interventional

device

Sponsor & Location

Hospital Clinico Universitario de Santiago

Santiago de Compostela, Spain

Timeline & Enrollment

N/A

Jun 15, 2022

Dec 31, 2023

90 participants

Primary Outcome

Difference in the first attempt intubation success rate (percentage)

Summary

Patients with anticipated difficult airway are recommended to be managed with an awake
 tracheal intubation. Initially fibreoptic bronchoscopy was considered the gold standard, but
 in the last decade videolaryngoscopes have been demonstrated to be an efficacy alternative
 technique. Recently, a systematic review and meta-analysis was published investigating the
 efficacy and safety of videolaryngoscopy compared with fibreoptic bronchoscopy for awake
 tracheal intubation. Eight prospective, randomized studies were included, with different
 videolaryngoscopes (C-MAC, GlideScope, Pentax AWS, McGraft, and Bullard). However, a direct
 comparison of two different videolaryngoscopes for awake tracheal intubation in patients with
 anticipated difficult airway has not been performed.

ICD-10 Classifications

Failed or difficult intubation
Failed or difficult intubation during labour and delivery
Failed or difficult intubation during pregnancy
Failed or difficult intubation during the puerperium
Respiratory arrest

Data Source

ClinicalTrials.gov

NCT05428995

Device Trial