Use of neonatal chest ultrasound to predict noninvasive ventilation failure.
Francesco Raimondi, Fiorella Migliaro, Angela Sodano...
https://pubmed.ncbi.nlm.nih.gov/25180278Actively Recruiting
Led by Hackensack Meridian Health · Updated on 2026-05-22
300
Participants Needed
1
Research Sites
N/A
Total Duration
Respiratory problems are a major challenge for newborns, especially late-preterm infants born between 34 and 36 weeks gestation. These infants face risks similar to more premature babies but may not always be born in hospitals with specialized neonatal care. This research aims to evaluate the usefulness of early point-of-care lung ultrasound (LUS) in predicting respiratory difficulties within the first 48 hours of life in these late-preterm newborns. It also compares the accuracy of three different lung ultrasound scoring systems to see which best predicts respiratory problems. In this observational study, babies born late-preterm who are initially breathing room air or receiving low-flow oxygen through a nasal cannula will receive a lung ultrasound within their first 4 hours of life. The ultrasound images will be scored using three established scoring methods. The babies will be monitored during their hospital stay to watch for any signs of respiratory distress or need for increased respiratory support during the first 48 hours after birth. Participants will be followed closely in the neonatal intensive care unit or well-baby nursery to track the onset and severity of breathing difficulties, including how soon respiratory support is needed and how long it is required. Researchers will use these observations to assess how well the lung ultrasound scores predict respiratory worsening. The study will also look at the need for invasive respiratory support and the timing of respiratory distress signs. The trial will continue through the initial hospital stay, aiming to improve early identification of at-risk late-preterm infants.
CONDITIONS
Predictive Value of Lung Ultrasound for Respiratory Decompensation in Late Preterm Neonates
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Within the first 4 hours of life
Participants undergo point-of-care lung ultrasound within the first 4 hours of life to assess lung status using three established scoring systems.
1 visit (in-person)
Duration - Up to 48 hours
Participants are monitored during initial hospitalization for respiratory decompensation and need for respiratory support within the first 48 hours of life.
Continuous monitoring during hospitalization
Total: 1 location
1
Hackensack Univeristy Medical Center
Hackensack, New Jersey, United States, 07601
Actively Recruiting
J
Jeanette Haugh
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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