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ETI During Intubation (SL)

I

International Institute of Rescue Research and Education

Status

Completed

Conditions

Intubation
Cardiac Arrest

Treatments

Device: Standard tracheal tube
Device: ETView VivaSight SL

Study type

Interventional

Funder types

Other

Identifiers

NCT02295618
ETI/2014/41

Details and patient eligibility

About

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.

Enrollment

107 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

107 participants in 2 patient groups

ETI with chest compressions
Experimental group
Description:
endotracheal intubation (ETI) during child mannikin resuscitation with uninterrupted chest compressions. In order to simulate the difficulties associated with intubation during uninterrupted chest compressions, CPR was performed by using LUCAS-2 (Physio-Control, Redmond, WA, U.S.).
Treatment:
Device: ETView VivaSight SL
Device: Standard tracheal tube
ETI without chest compressions
Experimental group
Description:
Endotracheal intubation of child mannikin during resuscitation without chest compressions.
Treatment:
Device: ETView VivaSight SL
Device: Standard tracheal tube

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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