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Comparison Four Intubation Devices

Comparison of Tracheal Intubation Using the Miller, Macintosh, Phillips and Wis-Hipple Blades During Infant Resuscitation: A Randomized Crossover Simulation Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02280213
Enrollment
145
Registered
2014-10-31
Start date
2014-11-30
Completion date
2015-01-31
Last updated
2015-02-03

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

Conditions

Intubation

Brief summary

Comparison of four laryngoscope blades (Miller, Macintosh, Phillips and Wis-Hipple) for infant intubation during resuscitation with and without chest compressions.

Interventions

DEVICEMIL

Direct laryngoscopy 1

DEVICEMAC

Direct laryngoscopy 2

DEVICEWIS

Direct laryngoscopy 3

DEVICEPHIL

Direct laryngoscopy 4

Sponsors

International Institute of Rescue Research and Education
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* give voluntary consent to participate in the study * paramedics * no clinical experience in infant intubation

Exclusion criteria

* not meet the above criteria * wrist or low back diseases * pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Time to intubation1 daytime from insertion of the blade to the first manual ventilation of the manikin´s lungs. If time of intubation is over than 60 seconds, attempt was recognized as failure.

Secondary

MeasureTime frameDescription
Cormack-Lehane grading1 dayself-reported percentage the vocal cord visualization using the Cormack-Lehane grading (grade 1-4)
dental compression1 daypressure applied on the upper teeth (n=none, mild=1, moderate=2, severe=3)
Success of intubation1 dayeffectiveness of the first, second and third intubation attempts and overall effectiveness of intubation by participants using four intubation devices. If the examinee failed at all attempts, the case was excluded from the time calculations.
Ease of Use1 dayTo access subjective opinions about the difficulty of the each intubation method, participants were asked to give a rating on a visual analogue scale (VAS) with a score from 1 (extremely easy) to 10 (extremely difficult).
POGO score1 dayThe POGO score describes how much glottic opening is visible. A POGO score of 100% indicates visualization of the entire glottic opening from the anterior commissure of the vocal cords to the interarytenoid notch. A POGO score of 0% corresponds with no visualization of laryngeal structures.

Countries

Poland

Outcome results

None listed

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