MedTrace Logo

Predicting the Need for Prolonged Respiratory Support in Neonates Delivered in a Lower-Level NICU Setting

NCT07344714 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2026-03-18

No results posted yet for this study

Summary

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

  • Respiratory Distress Syndrome, Newborn
  • Respiratory Distress Syndrome in Premature Infant
  • Transient Tachypnea of the Newborn
  • Meconium Aspiration Syndrome
  • Pneumonia Neonatal
  • Hyaline Membrane Disease
  • Pneumothorax
  • Respiratory Distress Neonatal

Sponsors & Collaborators

Principal Investigators

  • William A. Carey, MD · Mayo Clinic

Eligibility

Min Age
32 Weeks
Max Age
41 Weeks
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-03-11
Primary Completion
2026-10-31
Completion
2026-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07344714 on ClinicalTrials.gov