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Compare Outcomes of CPR Between the Video-laryngoscopy (VL) Users and the Direct-laryngoscopy (DL) Users

Improvement of Recovery of Spontaneous Circulation and Survival Using the Video-laryngoscopy for out-of Hospital Cardiac Arrest Patient

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03256019
Enrollment
600
Registered
2017-08-21
Start date
2011-03-01
Completion date
2016-03-01
Last updated
2017-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiopulmonary Arrest

Keywords

intubation, Cardiopulmonary Resuscitation

Brief summary

This is a clinical study based on the analysis of video-clip data of cardiopulmonary resuscitation (CPR) and clinical data for out of hospital cardiac arrest patients between 2011 and 2015. Aim of study is to compare the endotracheal intubation performance and CPR outcomes between videolaryngoscopy (VL) and direct laryngoscopy (DL) users.

Detailed description

Endotracheal intubation (ETI) has been considered to be the best method of airway management during cardiopulmonary resuscitation (CPR). However ETI during CPR is a highly skill-dependent procedure, then it should be attempted only highly trained physicians. Because of technical difficulty in using direct laryngoscopy (DL), various types of videolaryngoscopy (VL) devices using micro-camera technology have been designed to overcome the problems of DL. This study tried to compare the recovery of spontaneous circulation (ROSC) and survival discharge between use of standard device (DL) and VL in a real clinical setting. In addition, this study also compare the first pass success rate of ETI,speed of ETI, incidences of complications, and chest compression interruptions during cardiopulmonary resuscitation between both device users.

Interventions

PROCEDUREEndotracheal Intubation

Insertion of endotracheal tube into the trachea and supply oxygen using the Ambu-bagging during cardiopulmonary resuscitation

Sponsors

Konkuk University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who suffer sudden out-of hospital cardiac arrest

Exclusion criteria

* Cardiac arrests from multiple trauma * Cases of requesting the do-not attempt resuscitation before ETI * Intubated cases before arrival to emergency department

Design outcomes

Primary

MeasureTime frameDescription
Survival with good neurologic outcome6 months after emergency department visitSurvived patients who were conscious and able to perform independent activities of daily life (CPC1 or CPC2)

Secondary

MeasureTime frameDescription
ROSCwithin 1 hour after emergency department visitRecovery of spontaneous circulation by successful resuscitation
total time to complete ETI from the beginningwithin 1 hour after emergency department visittime from the advancement of the blade into the patient's mouth to the delivery of the first successful ventilation using the bag
complicationwithin 1 hour after emergency department visitPresence of chest compression interruption, esophageal intubation and dental injuries

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026