Actively Recruiting

Age: 34Weeks - 36Weeks
All Genders
NCT07216053

Predictive Value of Lung Ultrasound for Respiratory Decompensation in Late Preterm Neonates

Led by Hackensack Meridian Health · Updated on 2025-11-10

300

Participants Needed

1

Research Sites

103 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Respiratory morbidity presents a significant clinical challenge in the neonatal period, and an individual patient's clinical course is often difficult to predict. This is especially true for late-preterm infants, who share some of the same risks of premature babies in terms or respiratory morbidity, but whose births may not always be attended by a neonatologist, or who may be born at hospitals with lower level Neonatal Intensive Care Units (NICUs) and require transfer if they decompensate. With this study, the aim is to 1) determine the efficacy of early point of care lung ultrasound (LUS) to predict respiratory decompensation in the first 48 hours of life in late preterm infants and 2) to compare the performance of three lung ultrasound scoring systems, 3 type-of-lung, high risk pattern and total LUS scoring systems.

CONDITIONS

Official Title

Predictive Value of Lung Ultrasound for Respiratory Decompensation in Late Preterm Neonates

Who Can Participate

Age: 34Weeks - 36Weeks
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Infants born between 34 weeks 0 days and 36 weeks 6 days gestational age
  • Breathing room air or receiving nasal cannula oxygen at 1 litre per minute or less
  • Admitted to Neonatal Intensive Care Unit or Well Baby Nursery
Not Eligible

You will not qualify if you...

  • Born before 34 weeks or after 36 weeks 6 days gestational age
  • Presence of major genetic anomaly or syndromic condition
  • Having cardiac or pulmonary structural defects
  • Cord blood pH less than 7.0 or APGAR score of 5 or less at 5 minutes
  • Suspected fetal hemorrhage or significant anemia at birth

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hackensack Univeristy Medical Center

Hackensack, New Jersey, United States, 07601

Actively Recruiting

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Research Team

J

Jeanette Haugh

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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