Cerebral oxygenation during neonatal intubatio

Not Applicable

Completed

• Conditions: Respiratory distress; Cerebral blood flow; Reproductive Health and Childbirth - Complications of newborn

• Registration Number: ACTRN12619001276145
• Lead Sponsor: Royal Women's Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-09-16
• Study Completion: 2021-04-21
• Last Update Posted: 28 February 2022

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1.Any neonate undergoing endotracheal intubation in the delivery room or NICU AND
2.HR >120bpm at the time of randomisation
3. Prospective consent obtained from parent/guardian
4. Participation in the study ACTRN12618001498280

Exclusion Criteria

1.Requirement for immediate endotracheal intubation as determined by the treating clinician, without time for randomisation and potential application of nHF, eg. active cardiopulmonary resuscitation
2.Heart rate <120 bpm at the time of randomisation
3.Contraindication to nHF use (eg. congenital nasal anomaly, congenital diaphragmatic hernia, abdominal wall defects)
4.Nasal intubation planned

Study & Design

• Study Type: Observational
• Study Design: Not specified