• Scand J Trauma Resus · Jan 2015

    Randomized Controlled Trial Comparative Study

    The C-MAC videolaryngoscope compared with conventional laryngoscopy for rapid sequence intubation at the emergency department: study protocol.

    • Simon Sulser, Dirk Ubmann, Martin Brueesch, Georg Goliasch, Burkhardt Seifert, Donat R Spahn, and Kurt Ruetzler.
    • Institute of Anaesthesiology, University and University Hospital Zurich, Zurich, Switzerland. simon.sulser@usz.ch.
    • Scand J Trauma Resus. 2015 Jan 1;23:38.

    BackgroundEspecially in the emergency setting, rapid and successful airway management is of major importance. Conventional endotracheal intubation is challenging and requires high level of individual skills and experience. Videolaryngoscopes like the C-MAC are likely to offer better glottis visualization and serve as alternatives to conventional endotracheal intubation. The aim of this study is to compare clinical performance and feasibility of the C-MAC videolaryngoscope compared to conventional endotracheal intubation in the emergency setting.Methods/DesignThis study is designed as a prospective, patient-blinded, mono-center, randomized cohort study. This study will be performed at the Emergency Department of the University Hospital Zurich, Zurich, Switzerland. All patients transferred to the Emergency Department and requiring emergent endotracheal intubation will be screened. Successful intubation with first intubation attempt will serve as the primary outcome. Time to intubation, intubation attempts, Cormack & Lehane Score, ease of intubation, complications, necessity of using alternate intubation device, maximum drop of saturation, and potential technical problems serve as secondary outcomes.DiscussionIn the clinical setting, the ultimate success rate of endotracheal intubation ranges between 97% and 99%. Unexpected difficulties during laryngoscopy and poor glottis visualization occur in up to 9% of all cases. In these cases, videolaryngoscopes may increase success rate of initial intubation attempt and thereby patient safety.Trial Registrationwww.clinicaltrials.gov (identifier NCT02297113 ).

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