We expect that video-assisted intubation (video laryngoscopy) by ambulance nurses will have a higher success rate than intubation with a classical intubation device (direct laryngoscopy).
ID
Bron
Verkorte titel
Aandoening
Resuscitation requiring emergency endotracheal intubation
Ondersteuning
Erasmus Medical Center, Medical Research Ethics Committee (MREC)
AmbulanceZorg Rotterdam Rijnmond
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
First-time success
Achtergrond van het onderzoek
BACKGROUND
Literature shows that the rate of first-time success of emergency endotracheal intubation by ambulance nurses is highly variable; rates between 46 and 95% have been reported. Due to differences in device design, we hypothesize that the rate of first-time success can be improved when using videolaryngoscopy instead of direct laryngoscopy.
AIM
The primary aim of this prospective, observational study is to compare the rate of first-time success of intubation (by ambulance nurses) using videolaryngoscopy versus direct laryngoscopy. Secondary aims are to assess the rate of second-attempt success, time required for intubation, rate of adverse events, and rate of ROSC after videolaryngoscopy versus direct laryngoscopy, performed by ambulance nurses.
STUDY DESIGN
Observational study.
POPULATION
Patients requiring emergency endotracheal intubation.
INTERVENTION
Videolaryngoscopy
CONTROL
Direct laryngoscopy
ENDPOINTS
Primary outcome measure: first-time success.
Secondary outcome measures: second-attempt success, time required for intubation, adverse events, and ROSC.
Primary and secondary outcomes will be determined on-scene immediately after intubation.
RECRUITING COUNTRIES
The Netherlands
Doel van het onderzoek
We expect that video-assisted intubation (video laryngoscopy) by ambulance nurses will have a higher success rate than intubation with a classical intubation device (direct laryngoscopy).
Onderzoeksopzet
On-scene, immediately after intubation
Onderzoeksproduct en/of interventie
Videolaryngoscopy versus direct laryngoscopy
Algemeen / deelnemers
's-Gravendijkwal 230, 3015 CE Rotterdam
M.H.J. Verhofstad
P.O. Box 2040, 3000 CA Rotterdam
Rotterdam
The Netherlands
+31-10 7031050
m.verhofstad@erasmusmc.nl
Wetenschappers
's-Gravendijkwal 230, 3015 CE Rotterdam
M.H.J. Verhofstad
P.O. Box 2040, 3000 CA Rotterdam
Rotterdam
The Netherlands
+31-10 7031050
m.verhofstad@erasmusmc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Patient requiring endotracheal intubation
2. GCS of 3 points, without suspected neurological injuries
3. Estimated age 18 years or older
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. No CO2 production visible on capnogram, or no capnogram available
Opzet
Deelname
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Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
Register | ID |
---|---|
NTR-new | NL5582 |
NTR-old | NTR6174 |
Ander register | : MEC-2015-467 (METC Erasmus MC) |