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KoMAC Videolaryngoscope for Double-lumen Intubation

Comparison of the KoMAC Videolaryngoscope With the Macintosh Laryngoscope for Double-lumen Intubation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03677505
Enrollment
60
Registered
2018-09-19
Start date
2018-10-05
Completion date
2020-03-02
Last updated
2020-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intubation

Keywords

double lumen intubation, videolaryngoscope

Brief summary

KoMAC videolaryngoscope is a portable intubating device with an angulated single-use blade of adjustable size and a liquid crystal display monitor mounted on top of the handle, which is similar in shape to the McGrath videolaryngoscope. The purpose of this study was to evaluate the efficacy of the KoMAC videolaryngoscope for double-lumen intubation regarding intubation time, laryngeal view and ease of intubation, compared to Macintosh laryngoscope.

Interventions

DEVICEKoMAC videolaryngoscope

Double lumen endotracheal intubation was performed with the KoMAC videolaryngoscope

DEVICEMacintosh Laryngoscope

Double lumen endotracheal intubation was performed with the Macintosh Laryngoscope

Sponsors

Ajou University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* patients scheduled for thoracic surgery requiring one lung ventilation

Exclusion criteria

* predicted difficult airway * rapid sequence intubation * cervical injury

Design outcomes

Primary

MeasureTime frameDescription
Intubation timefrom 2 min after rocuronium injection to completion of intubation (time interval is about 120 seconds)Time interval between laryngoscope passing the teeth to the confirming of end tidal CO2

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026