Can ultrasound prevent aspiration in injured kids?
NCT ID NCT05330351
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether ultrasound can accurately measure stomach contents in children with traumatic injuries who need emergency surgery. Researchers will compare ultrasound estimates with actual stomach fluid drained after intubation. The goal is to better predict aspiration risk and guide anesthesia choices.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could provide a non-invasive way to assess aspiration risk in pediatric trauma patients before anesthesia.
- What could go wrong
- This is a small, early-stage study with only 40 participants, so results may not apply to all children. The ultrasound method may not be accurate enough to replace current practices.
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.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2022
- Expected to finish
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Dec 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
perioperative pediatric trauma patients
- Ages
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0 to 17 years
- Sex
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Anyone
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: * Pediatric patients ages 0-17 years-old * Patients suffering from a traumatic injury requiring urgent or emergent surgery. * Inpatient or Same-Day Surgery Exclusion Criteria: * Children with altered or abnormal gastric physiology, ie, history of Nissen Fundoplication, history of short-gut syndrome, history of bariatric surgery/gastric sleeve, history of gastroparesis or functional dysmotility, etc.
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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.
Contacts and locations
Locations
-
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, 19104, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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