Actively Recruiting
Predicting the Need for Prolonged Respiratory Support in Neonates Delivered in a Lower-Level NICU Setting
Led by Mayo Clinic · Updated on 2026-03-18
500
Participants Needed
1
Research Sites
42 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to analyze the gastric fluid aspirated from the stomachs of neonates receiving routine post-delivery care to predict the need for prolonged respiratory support (\>6 hours of life).
CONDITIONS
Official Title
Predicting the Need for Prolonged Respiratory Support in Neonates Delivered in a Lower-Level NICU Setting
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Neonates born at 32 completed weeks gestational age or older whose deliveries are attended by the neonatal resuscitation team and for whom routine gastric suctioning is indicated
- Neonates whose parents actively accepted or did not actively decline the Minnesota Research Authorization.
You will not qualify if you...
- Neonates with known or suspected congenital anomalies
- Neonates for whom only comfort measures are planned or possible at time of delivery
- Neonates whose parents actively declined the Minnesota Research Authorization
- Neonates with other identifiable causes of respiratory distress including pneumothorax, meconium aspiration syndrome, or pneumonia.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Mayo Clinic in Rochester
Rochester, Minnesota, United States, 55905
Actively Recruiting
Research Team
L
Lavonne M. Liedl, LRT
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
0
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