Clinical Trials Directory

Trials / Completed

CompletedNCT05607836

IntuBrite Versus Macintosh for Endotracheal Intubation in Out of Hospital Cardiac Arrest

A Pilot, Prospective, Randomized Trial of IntuBrite Versus Macintosh Direct Laryngoscopy for Paramedic Endotracheal Intubation in Out of Hospital Cardiac Arrest

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
86 (actual)
Sponsor
Medical University of Lodz · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

a randomized, parallel, non-blinded trial in a single Emergency Mdeical Service in Poland within a group of 34 ground ambulances crews, comparing time and first pass success (FPS) for endotracheal intubation (ETI) in DL using the IntuBrite® (INT) and Macintosh laryngoscope (MCL) during cardiopulmonary resuscitation (CPR). intubations will be performed using INT and MCL based on an intention-to-treat analysis. The FPS time of the ETI attempt will be analysed. First attempt success will be counted.

Detailed description

Investigators designed a prospective observational study to compare INT (IntuBrite®, LLC; Vista, CA, USA) and MCL for ETI performed by paramedics in OHCA without an emergency physician on the scene. The main goal was to determine whether INT is superior to using an MCL laryngoscope during a tracheal intubation attempt in nontraumatic OHCA, in terms of time and effectiveness. The time of intubation was measured using an electronic stopwatch. Time measurement began when the paramedic held the selected laryngoscope and declared their readiness to perform the procedure. The effectiveness of the first ETI attempt for instrumental airway management for nontraumatic adult OHCA and end-tidal carbon dioxide monitoring was used to confirm correct device placement in all patients. The degree difficulty of intubation attempts for all of the patients included in the study. A long-term survival and a cost-effectiveness analysis were not included within this trial. The investigators will collect case report forms (CRFs) from patients after OHCA within a 40-month period. The average professional experience of the paramedics in instrumental airway management will be noted (DL and LMA). The primary outcome is the FPS time of the ETI attempt performed by the paramedics. The success rate on the first intubation attempt will be counted.

Conditions

Interventions

TypeNameDescription
DEVICEIntuBrite intubationUse of new laryngoscope IntuBrite for intubation in patients with cardiopulmonary arrest and during resuscitation
DEVICEMacintosh laryngoscopeUse of standard Macintosh blade laryngoscope for intubation in patients with cardiac arrest and requiring cardiopulmonary resuscitation

Timeline

Start date
2016-01-01
Primary completion
2020-01-01
Completion
2022-06-01
First posted
2022-11-07
Last updated
2022-11-07

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT05607836. Inclusion in this directory is not an endorsement.