Tiny study to probe nose Airflow's effect on brain waves in ventilated patients
NCT ID NCT07468266
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study will test whether a device that delivers airflow to the nose changes brain activity in 12 adults who are sedated and on a breathing machine after planned surgery. Researchers will measure brain waves using EEG to see if different airflow rates have different effects. The goal is to learn more about how nasal airflow influences the brain in this setting.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- F&P Tui device (nasal airflow)
- What this could lead to
- If successful, this could help understand how nasal airflow influences brain activity in ventilated patients, potentially guiding better care.
- What could go wrong
- This is a very small, early study (12 participants) that only measures brain signals, not patient outcomes. Results may not apply broadly.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Mar 2026
An estimate. Start dates often move.
- Expected to finish
-
Feb 2027
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults \>18 years of age * Receiving sedation via propofol and fentanyl * Undergoing surgical procedure with planned post-operative invasive ventilation Exclusion Criteria: * Pre-existing neurological injury or condition
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Invasive ventilation are added.
Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Department of Critical Care Medicine, Auckland City Hospital
Auckland, New Zealand
More trials for these conditions
Other studies related to the condition(s) this trial covers.