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New breathing method could ease stress for preterm infants

NCT ID NCT07418502

First seen Feb 19, 2026 · Last updated Jun 20, 2026 · Updated 20 times

Summary

This study tests whether a new breathing support called Pressure Targeted High Flow works as well as standard CPAP in premature infants. About 78 babies born before 33 weeks will try each method for 24 hours. Researchers will monitor breathing, oxygen needs, and comfort to see if the new approach is a viable alternative.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Ascension Seton Medical Center

    Austin, Texas, 78705, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

  • Sharp Mary Birch Hospital for Women & Newborns

    San Diego, California, 92123, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Pressure Targeted High Flow (a breathing support procedure)

What this could lead to

If it works, this could offer a more comfortable breathing support option for premature infants, potentially reducing stress and resource use.

What could go wrong

This is a small, early-phase trial with only 78 infants, so results may not apply broadly. The new method might not provide enough support, leading to breathing failure.

Conditions

The condition(s) this trial relates to.

bronchopulmonary dysplasia Premature Birth Pulmonary Atelectasis respiratory distress syndrome in premature infants

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.