Can gentle oscillations help premature babies breathe better?
NCT ID NCT01277874
First seen Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time
Summary
This trial tests whether adding gentle oscillations to standard nasal continuous positive airway pressure (NCPAP) improves breathing support for newborns with respiratory distress syndrome. Premature infants who need NCPAP will be randomly assigned to receive either oscillatory NCPAP or standard NCPAP. Researchers will compare how well each method stabilizes breathing, reduces the need for mechanical ventilation, and shortens the time on respiratory support.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Oscillatory nasal continuous airway pressure (Osc-NCPAP), a device that adds oscillations to standard NCPAP delivered via nasal prongs
- What this could lead to
- If oscillatory NCPAP works better than standard NCPAP, it could reduce the need for mechanical ventilation in premature infants and improve their breathing stability.
- What could go wrong
- This is an early-stage trial with a small number of participants, so results may not be conclusive. The added oscillations could also cause discomfort or other unforeseen issues in fragile newborns.
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.
- Start date
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Dec 2014
- Expected to finish
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Apr 2017
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.
- Ages
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Up to 28 days
- 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 Criteria: * Newborn (0-28 days of age) admitted to Neonatal Intensive Care Unit (NICU) * Ordered respiratory treatment of NCPAP Exclusion Criteria: * Major congenital defect * Known or suspected chromosomal disorder
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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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Primary Children's Medical Center
Salt Lake City, Utah, 84113, United States
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University of Utah Health Sciences Center
Salt Lake City, Utah, 84132, United States
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Valley Children's Healthcare
Madera, California, 93636, United States
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