About this trial

This prospective, multicenter observational study aims to evaluate the effect of different flow rates of high-flow nasal oxygen (HFNO) on the quality of the laryngoscopic view during videolaryngoscopy in adult patients undergoing general anesthesia. Each patient will serve as their own control, with repeated measurements obtained at three different HFNO flow settings (0, 40, and 60 L/min). The study will assess objective and subjective parameters of glottic visualization using standardized scoring systems.

Eligibility criteria

Qualifiers

Age ≥18 years

Scheduled for endotracheal intubation under general anesthesia

Use of videolaryngoscopy

Disqualifiers

Anticipated difficult airway

Emergency intubation

Contraindications to HFNO

Inability to obtain adequate video recording

Trial design

Treatments tested in this trial

  • HFNO flow 0
  • HFNO flow 40
  • HFNO 60

Treatment groups

150 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators

Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.

Lead sponsor