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ETI During Intubation

Can the ETView VivaSight SL Rival the Macintosh Laryngoscopy With Conventional Tube During Adult Resuscitation by Novice Physicians: a Randomized Crossover Simulation Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02295618
Acronym
SL
Enrollment
107
Registered
2014-11-20
Start date
2014-11-30
Completion date
2014-11-30
Last updated
2014-12-02

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

Conditions

Cardiac Arrest, Intubation

Brief summary

The objective of this study is to compared effectiveness of intubation using ETView VivaSight SL and standard tracheal tube during resuscitation performed by a novice-physicians.

Interventions

Intubation using Macintosh laryngoscope and standard tracheal tube

Intubation using ETView VivaSight SL

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 * maximum 1 year of work experience in medicine * maximum 10 clinical intubations

Exclusion criteria

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

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
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.
Cormack-Lehan scale1 dayself reported Cormack-Lehan scale during intubation

Countries

Poland

Outcome results

None listed

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