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Feasibility and Reliability of Synchronized Non-invasive Intermittent Positive Pressure Ventilation in Preterm Infants After Birth

NCT05399914 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2024-09-23

No results posted yet for this study

Summary

The aim of this prospective observational study (pilot study) is to test if synchronized noninvasive positive pressure ventilation (S-NIPPV) is feasible and works appropriately during transition from intrauterine to extrauterine life in very preterm infants in the delivery room.

Conditions

  • Preterm Infant
  • Delivery Room
  • Respiratory Support
  • Synchronized Noninvasive Positive Pressure Ventilation (SNIPPV)

Interventions

OTHER

S-NIPPV

Synchronized noninvasive positive pressure ventilation during the first 10 minutes after birth.

Sponsors & Collaborators

  • University Hospital Tuebingen

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-22
Primary Completion
2023-10-11
Completion
2023-10-11

Countries

  • Germany

Study Locations

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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 NCT05399914 on ClinicalTrials.gov