ClinicalTrials.gg
CompletedNCT02277951IDRUpdated Oct 29, 2014

Intubation During Resuscitation

An observational study in Intubation and Cardiopulmonary Resuscitation, sponsored by International Institute of Rescue Research and Education. Completed. Per ClinicalTrials.gov, last updated 2014-10-29.

Sponsored by International Institute of Rescue Research and Education · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
141
Sex
All
01

Study summary

The aim of the study was to compare time and success rates of four intubation devices ( in a cardiopulmonary scenario with uninterrupted chest compressions with a standardized manikin model.

The investigators hypothesized that fiberoscope laryngoscopes may improve success rates.

Read the detailed description

Devices using in study:

The Bonfils Intubation Fibrescope (BONFILS)(KARL STORZ Endovision, Inc., Charlton, MA, USA), The Video Rigid Flexing Laryngoscope (RIFL)( AI Medical Devices, Inc., Williamston, MI, USA), The C-MAC® S Video Laryngoscope Blade Mac#3(C-MAC®S) (KARL STORZ Endovision, Inc., Charlton, MA, USA) The Macintosh Laryngoscope Blade no. 3 (MAC) (LifeLine Medical, Inc., Brooksville, FL, USA).

02

Conditions studied

  • Intubation
  • Cardiopulmonary Resuscitation
03

In context

Lead sponsor

International Institute of Rescue Research and Education is the lead sponsor of 37 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
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Personnel of emergency medical services and hospital emergency units

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • experienced emergency personnel: nurses, paramedics

Exclusion criteria

Exclusion Criteria:

  • no experience in out-of-hospital emergency medicine
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
141 participants (actual)
Patient registry
No

Groups and cohorts

  • Participants

    The Bonfils Intubation Fibrescope the Video Rigid Flexing Laryngoscope the C-MAC® S Video Laryngoscope the Macintosh Laryngoscope

    Device: The Bonfils Intubation Fibrescope · Device: The Video Rigid Flexing Laryngoscope · Device: The C-MAC® S Video Laryngoscope · Device: The Macintosh Laryngoscope

Interventions

  • DeviceThe Bonfils Intubation Fibrescope

    Effectiveness and time to successful intubation will be measured.

  • DeviceThe Video Rigid Flexing Laryngoscope

    Effectiveness and time to successful intubation will be measured.

  • DeviceThe C-MAC® S Video Laryngoscope

    Effectiveness and time to successful intubation will be measured.

  • DeviceThe Macintosh Laryngoscope

    Effectiveness and time to successful intubation will be measured.

06

What researchers measure

Primary outcomes

  1. Time to successful intubation

    The devices to be compared include (1) The Bonfils Intubation Fibrescope , (2) the Video Rigid Flexing Laryngoscope, (3) the C-MAC® S Video Laryngoscope, (4) the Macintosh Laryngoscope. Successful intubation will be measured in the seconds from insertion of an intubation device to the first manual ventilation of the mannequin's lungs.

    Time frame: Subjects complete study in 1 day

  2. Success rate of ETI

    The devices to be compared include (1) The Bonfils Intubation Fibrescope , (2) the Video Rigid Flexing Laryngoscope, (3) the C-MAC® S Video Laryngoscope, (4) the Macintosh Laryngoscope. Successful intubation will be measured in the seconds from insertion of an intubation device to the first manual ventilation of the mannequin's lungs.

    Time frame: Subjects complete study in 1 day

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 29, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02277951
Lead sponsor
International Institute of Rescue Research and Education
Responsible party
Lukasz Szarpak (Lukasz Szarpak, National Institute of Cardiology, Warsaw, Poland) — Principal investigator
First posted
Oct 29, 2014
Start date
May 2014
Primary completion
Jul 2014
Completion
Jul 2014
Last update
Oct 29, 2014

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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

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Discussion

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