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Double Lumen Tube Intubation

Not Applicable
Conditions
Cardiac Arrest
Endotracheal Intubation
Interventions
Device: standard double-lumen tube
Device: VivaSight Double Lumen Tube
Registration Number
NCT02295657
Lead Sponsor
International Institute of Rescue Research and Education
Brief Summary

The aim of this study was to compare time, success rates of different double-lumen tubes in intubation in a standardized manikin model.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
120
Inclusion Criteria
  • give voluntary consent to participate in the study
  • minimum 1 year of work experience in emergency medicine
  • experienced emergency medicine personnel (physicians, nurses, paramedics)
Exclusion Criteria
  • not meet the above criteria
  • wrist or low back diseases

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
ETI intubationVivaSight Double Lumen Tubeendotracheal intubation in manikin
ETI intubationstandard double-lumen tubeendotracheal intubation in manikin
Primary Outcome Measures
NameTimeMethod
Success of intubation1 day

effectiveness of first, second and third intubation attempts and overall effectiveness of intubation by participants

Secondary Outcome Measures
NameTimeMethod
Cormack-Lehane grading1 day

self-reported percentage the vocal cord visualization using the Cormack-Lehane grading (grade 1-4)

Intubation time1 day

time in seconds required for a successful intubation attempt

Preferred ETI device1day

participants were asked which method of ETI they would prefer in a real-life.

Trial Locations

Locations (1)

International Institute of Rescue Research and Education

🇵🇱

Warsaw, Masovia, Poland

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