Nasal Airflow in Post-operative Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorFisher and Paykel Healthcare

About this trial

The goal of this investigation is to examine the effect of nasal airflow in invasively ventilated adult patients following planned surgery. The main questions it aims to answer are:

* Does the investigational device produce an effect measured by EEG? * Are there differences in effect with modified airflow states?

Eligibility criteria

Qualifiers

Adults >18 years of age

Receiving sedation via propofol and fentanyl

Undergoing surgical procedure with planned post-operative invasive ventilation

Disqualifiers

Pre-existing neurological injury or condition

Trial design

Treatments tested in this trial

  • TUI-1
  • TUI-2

Treatment groups

12 Participants
are divided into 2 treatment groups

Sponsors and collaborators