Last reviewed · How we verify

Visualization of the Intubation Pathway With the "IRRIS"-Device

NCT03234283 NA COMPLETED

A prospective, open label, non-randomized, single centre safety and feasibility study. Patients with no expected airway difficulties scheduled for elective surgery including tracheal intubation and general anesthesia procedures will be enrolled into the study. Following standard induction of anesthesia, the IRRIS will be attached to the patient's neck skin just beneath the laryngeal prominence (Adam's apple) and the intubation will be performed by using a video-laryngoscope in a standardized fashion. The IRRIS device emits a light that penetrates through the skin into the airway and that is visible on the video-laryngoscope display. This light highlights the right pathway for the tracheal tube and facilitates the visual recognition and identification of the laryngeal inlet. In case of problems identified during the induction period such as an unexpected difficult intubation situation and the IRRIS does not provide the expected facilitation of intubation, the local "unexpected difficult airway" protocol goes into effect.

Details

Lead sponsorUniversity of Zurich
PhaseNA
StatusCOMPLETED
Enrolment40
Start dateSat Jul 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionTue Nov 14 2017 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Switzerland