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ETI During Spinal Trauma

I

International Institute of Rescue Research and Education

Status

Unknown

Conditions

Intubation
Cardiac Arrest

Treatments

Device: Standard tracheal tube
Device: ETView VivaSight SL

Study type

Interventional

Funder types

Other

Identifiers

NCT02295631
ETI/2014/42

Details and patient eligibility

About

The aim of this study was to compare time, success rates of different tracheal tubes (standard tube and ETView VivaSight SL) for intubation with an immobilized cervical spine in a standardized manikin model.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

150 participants in 2 patient groups

ETI during immobilized spine (oral intubation)
Experimental group
Description:
intubation with immobilized cervical spine endotracheal intubation with immobilized cervical spine
Treatment:
Device: ETView VivaSight SL
Device: Standard tracheal tube
ETI during immobilized spine (nasal intubation)
Experimental group
Description:
intubation with immobilized cervical spine endotracheal intubation with immobilized cervical spine
Treatment:
Device: ETView VivaSight SL
Device: Standard tracheal tube

Trial contacts and locations

1

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Central trial contact

Andrzej Kurowski

Data sourced from clinicaltrials.gov

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