AI-Powered oxygen device could revolutionize respiratory care
NCT ID NCT06952816
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new AI device called EMILY that automatically adjusts oxygen levels for people with acute or chronic respiratory failure. Researchers will enroll 20 adults in the hospital to see how well the device keeps oxygen in a safe range and how quickly it responds to changes. The goal is to improve patient safety and reduce the need for constant manual adjustments by medical staff.
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 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Apr 2025
- Expected to finish
-
Dec 2026
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: * Men and women over 18 years of age. * Admitted to intermediate respiratory care unit with a diagnosis of acute respiratory failure for at least 8 hours. * Informed consent understood and signed. Exclusion Criteria: * Hemodynamic instability. * Severe temperature changes. * Hemoglobinopathies, severe anemia, severe acidosis, or severe alkalosis. * Anatomical disturbances. * Pregnancy or breastfeeding.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Acute respiratory failure are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
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
2 sites. 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
-
Hospital Universitario Fundación Jiménez Díaz
RECRUITINGMadrid, Spain
-
Hospital Universitario Fundación Jiménez Díaz
RECRUITINGMadrid, Spain
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A chest belt that maps the lungs could help breathing machines fit better
- A global effort to make moving critically ill patients safer
- Healing together: could a Couples-Based program ease ICU aftermath?
- Are ventilated patients starving in silence? a new study investigates
- Can a simple inhaled combo keep pneumonia patients off ventilators?
- Can a Diaphragm-Sensing ventilator mode reduce breathing asynchrony?