CClinicalTrials.gg
Status unknownNCT02289638Updated Nov 13, 2014

Effectiveness of Child Intubation

An interventional study of Intubrite and MIL in Cardiac Arrest, sponsored by International Institute of Rescue Research and Education. Status unknown at 1 site in Poland. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2014-11-13.

Sponsored by International Institute of Rescue Research and Education · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Nov 2014), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

We hypothesized that the Intubrite Video Laryngoscope System VLS 6600 is beneficial for intubation of pediatric manikins while performing CPR. In the current study, we compared effectiveness of the Intubrite and MIL laryngoscopes in child resuscitation with and without CC.

02

Conditions studied

  • Cardiac Arrest

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Keywords

  • intubation
03

In context

Heart Arrest

966 studies on the registry are indexed under Heart Arrest; 227 are open to participants now.

This study's planned enrollment of 100 is close to the median of 100 across 557 interventional studies indexed under Heart Arrest.

Browse Heart Arrest studies →

Lead sponsor

International Institute of Rescue Research and Education is the lead sponsor of 36 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Give voluntary consent to participate in the study
  • minimum 1 year of work experience in emergency medicine
  • experienced emergency medical personnel (physicians, nurses, paramedics)

Exclusion criteria

Exclusion Criteria:

  • Not meet the above criteria
  • Wrist or Low back diseases
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Intubation without chest compressions

    Endotracheal intubation of pediatric mannikin during resuscitation without chest compressions.

    Device: Intubrite · Device: MIL

  • Experimental
    Intubation with uninterrupted chest compressions

    Endotracheal intubation of pediatric mannikin during 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.).

    Device: Intubrite · Device: MIL

Interventions

  • DeviceIntubrite

    Video-Laryngoscopy

    Also known as: Intubrite Video Laryngoscope System VLS 6600

  • DeviceMIL

    Direct-Laryngoscopy

    Also known as: Miller Laryngoscope

06

What researchers measure

Primary outcomes

  1. Success of intubation

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

    Time frame: 1 day

Secondary outcomes

  1. Intubation time

    time in seconds required for a successful intubation attempt

    Time frame: 1 day

  2. POGO score

    self-reported percentage of glottis opening (POGO) score

    Time frame: 1 day

  3. Cormack-Lehane grading

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

    Time frame: 1 day

07

Study locations

1 of 1 sites recruiting
  • International Institute of Rescue Research and Education
    Warsaw, Masovia 03-122, Poland
    • Lukasz Szarpak · Contact · lukasz.szarpak@gmail.com · +48500186225
    • Lukasz Szarpak · Principal investigator
    • Andrzej Kurowski · Sub investigator
    • Lukasz Czyżewski · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 13, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02289638
Lead sponsor
International Institute of Rescue Research and Education
Responsible party
Lukasz Szarpak (Institute of Cardiology, Warsaw, Poland, International Institute of Rescue Research and Education) — Principal investigator
First posted
Nov 13, 2014
Start date
Nov 2014
Primary completion
Nov 2014 (estimated)
Completion
Nov 2014 (estimated)
Last update
Nov 13, 2014

Study contacts

Andrzej Kurowski
Contact
andrzejkurowski987@gmail.com
+48500186225
Lukasz Szarpak
principal investigator · Institute of Cardiology

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2014. You cannot join it, but the record below documents what was studied.

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