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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
150
conventional endotracheal intubation
University Hospital Zuerich, Dept of Anesthesiology
Zurich, Canton of Zurich, Switzerland
Success Rate
defined as successful placement of endotracheal tube within the trachea and
Time frame: 10 minutes
time to intubation
defined as time between insertion of the videolaryngoscope/ Macintosh blade into the mouth until detection of end-tidal CO2
Time frame: 10 minutes
Laryngoscopic view
Cormack and Lehane Score
Time frame: 10 minutes
Number of intubation attempts
Time frame: 10 minutes
Unrecognized esophageal intubation
Time frame: 10 minutes
Ease of intubation (1-5)
o (1) very easy, (2) easy, (3) somewhat difficult, (4) difficult, (5) impossible
Time frame: 10 minutes
Violations of the teeth
number of patients; teeth will be inspected for potential damage and documented accordingly
Time frame: 10 minutes
Necessity of using further, alternative airway devices for successful intubation (if randomized airway device failed)
number of patients, requiring alternate device
Time frame: 10 minutes
Maximum drop of saturation
Spo2 will be measured continuously and documented accordingly
Time frame: 10 minutes
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