Ultrasound-Guided baby positioning may cut pneumonia risk in ventilated newborns
NCT ID NCT07254507
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether using lung ultrasound to guide how nurses position ventilated newborns can prevent pneumonia better than standard repositioning every two hours. Researchers enrolled 80 full-term infants on breathing machines. The goal was to see if personalized positioning based on ultrasound images lowers the rate of ventilator-associated pneumonia.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lung ultrasound-guided posture management
- What this could lead to
- If effective, this approach could reduce pneumonia rates in ventilated newborns, improving outcomes without drugs.
- What could go wrong
- This is a small, completed study with 80 infants, so results may not apply broadly. The intervention is behavioral, not a drug, so impact may be modest.
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
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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
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80 people
The number who actually took part.
- Started
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Jan 2024
- Finished
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Oct 2025
- 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.
- Ages
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1 hour to 3 months
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Eligible participants included term neonates (gestational age 37-42 weeks) who required invasive mechanical ventilation for more than 48 hours. Exclusion Criteria: * Exclusion criteria included ①preterm neonates; ② Neonates with early sepsis or previous pneumonia;③ Not suitable for patients with enteral nutrition;④ Newborns requiring mechanical ventilation due to surgery;⑤ There are many infants with congenital abnormalities or suspected chromosomal abnormalities.
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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
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The Second People's Hospital of Guangdong Province affiliated to Jinan University
Guangzhou, Guangdong, 510317, China
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Other studies related to the condition(s) this trial covers.
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