Actively Recruiting
Neonatal Intestinal Obstruction: Prenatal Factors and Postnatal Outcomes
Led by Meyer Children's Hospital IRCCS · Updated on 2026-02-25
60
Participants Needed
1
Research Sites
90 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Neonatal intestinal obstruction is one of the most common surgical emergencies in newborns. In some cases, signs of possible intestinal obstruction can already be detected during pregnancy through prenatal ultrasound. However, not all prenatal ultrasound findings accurately predict whether a newborn will truly have an intestinal obstruction after birth. The purpose of this retrospective observational study is to evaluate which prenatal ultrasound findings are most strongly associated with confirmed intestinal obstruction after birth. In particular, the study aims to identify a specific cutoff value for fetal bowel dilation that best predicts postnatal intestinal obstruction. Other prenatal ultrasound features, such as excess amniotic fluid (polyhydramnios), ascites, echogenic bowel, and other abdominal findings, will also be analyzed. The study will include newborns with a prenatal suspicion of intestinal obstruction who were evaluated at Meyer Children's Hospital between January 2016 and December 2024. Researchers will review existing medical records and ultrasound data. No additional tests or interventions will be performed for study purposes. The results of this study may help improve prenatal counseling, optimize delivery planning in specialized centers, and support early postnatal management of newborns at risk for intestinal obstruction.
CONDITIONS
Official Title
Neonatal Intestinal Obstruction: Prenatal Factors and Postnatal Outcomes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Neonates from singleton pregnancies with prenatal ultrasound suspicion of intestinal obstructive pathology
- Availability of complete postnatal follow-up data
You will not qualify if you...
- Missing delivery data
- Missing prenatal ultrasound data
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Aou Meyer IRCSS
Florence, Florence, Italy, 50139
Actively Recruiting
Research Team
A
Antonino Morabito
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
2
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