Clinical Trials Directory

Trials / Completed

CompletedNCT02297113

Rapid Sequence Intubation at the Emergency Department

The C-MAC Videolaryngoscope Compared With Conventional Laryngoscopy for Rapid Sequence Intubation at the Emergency Department

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

Summary

All patients undergoing emergent endotracheal intubation (RSI) at the Emergency Department will be screened for inclusion in this clinical study. The indication of endotracheal intubation is an exclusively clinical decision and is not affected by this study protocol in any aspect. If fulfilling the In- and exclusion criteria's, patient will be randomly assigned to one of two groups 1. C-MAC Videolaryngoscope in appropriate size 2. conventional endotracheal intubation using Macintosh Blade in appropriate size Randomization (1:1) will be based on computer-generated codes maintained in sequentially numbered opaque envelopes that will be opened immediately before randomization.

Conditions

Interventions

TypeNameDescription
DEVICEMacintosh bladeconventional endotracheal intubation
DEVICEC-MAC videolaryngoscope

Timeline

Start date
2014-11-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2014-11-21
Last updated
2016-03-25

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT02297113. Inclusion in this directory is not an endorsement.