Ultrasound-detectable Endotracheal Tube: a Feasibility Study
Recruiting now · Not applicable
Conditions studied: Cardiac Catheterization, Endotracheal Tube
In brief
The researchers are studying whether special features make it easier to see if the breathing tube is in the correct place. It is hoped that the investigational device will enable more accurate placement (depth and trachea vs. esophagus).
Key facts
- Study ID
- NCT05941013
- Run by
- John R. Charpie
- People needed
- 20
- Starts
- 2023-11-15
- Expected to finish
- 2027-04-01
- Last updated by the study team
- 2026-02-05
Who can join
Age: 1 and older, up to 4. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient is undergoing scheduled or planned diagnostic or interventional cardiac catheterization with planned general anesthesia requiring endotracheal intubation.
You may not qualify if…
- Patient has a known airway abnormality, including tracheal stenosis, previous tracheal stenosis, or tracheobronchomalacia.
- Patient has a tracheostomy.
- Patient is ventilator-dependent.
- Patient has an anticipated difficult intubation based upon airway exam and/or history of difficult intubation.
- Patient is unlikely (in opinion of anesthesia team) or is unable to be intubated with 3.5 mm, 4.0 mm, or 4.5 mm Inner Diameter USD-ETT due to the size of the patient or their airway.
- Patient is already intubated prior to the scheduled procedure.
- It is anticipated that the patient will not be extubated after the catheterization procedure.
- Concurrent enrollment in another clinical trial with an intervention during the cardiac catheterization procedure or 30 days afterwards.
- Allergy to plastic/materials in USD-ETT
Where it is running
- University of Michigan — Ann Arbor, Michigan, United States (enrolling)
Full record on ClinicalTrials.gov
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