Bedside ultrasound could predict breathing problems when removing tracheostomy tubes
NCT ID NCT07306091
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a bedside ultrasound can predict breathing problems before removing a tracheostomy tube in critically ill patients. Researchers will measure vocal cord movement and airflow in 107 ICU patients and compare ultrasound results with standard exams. The goal is to see if ultrasound can safely guide the decision to remove the tube.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ultrasound device
- What this could lead to
- If successful, this could make removing tracheostomy tubes safer and more predictable for critically ill patients.
- What could go wrong
- This is a small, early-stage study with only 107 participants, so results may not apply to all patients. Ultrasound may not detect all airway problems.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 107 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2024
- Expected to finish
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Feb 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
critically ill patients whom suitable for decanulation after tracheostomy
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Criterias 1. Critically ill patients (CIPs) who are receiving treatment within the specified time period and who require a tracheostomy. 2. Critically ill patients who are suitable for decannulation (underwent spontaneous breathing trials with the use of CPAP ( CPAP level of maximum 6 cm of water and maximum 10 cm of water pressure support at least 24 hours ). 3. Critically ill patients with intact swallowing reflexes ( patients were first examined for GAG reflexes, followed by ultrasonography; changes in muscle length and contraction velocity during swallowing were measured in a sagittal section using a convex probe , 4. CIPs with GCS\>8. Exclusion Criteria: 1.Critically ill patients under 18 years of age. 2.Critically ill patients who do not require tracheostomy. 3.Critically ill patients who are spontaneously breathing and can be weaned off the ventilator for \<24 hours 4.Critically ill patients with GCS \< 8. 5.Critically ill patients with absent swallowing reflexes \-
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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.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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
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Uludag Universty Faculty of MedicineDepartment of Anesthesiology and Reanimation, Bursa, Turkey
Bursa, 16140, Turkey (Türkiye)
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