A first in human study for a new resuscitation monitor for newborn babies requiring resuscitation at birth
- Conditions
- eonates requiring resuscitation with manual positive pressure ventilation following birth.Neonates requiring resuscitation with manual positive pressure ventilation following birth.Reproductive Health and Childbirth - Complications of newbornEmergency medicine - Resuscitation
- Registration Number
- ACTRN12622000250730
- Lead Sponsor
- ResusRight Pty Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Neonatal participants: There are two groups of neonatal participants for this study.
Neonatal Group 1 - Resuscitation at birth
Neonates born from 30 weeks gestation that require manual positive pressure ventilation during resuscitation following birth will be recruited to the study.
Neonatal Group 2 - Neonatal Intensive Care Neonates
Neonates from 26 weeks gestation that are admitted to the NICU that require manual
positive pressure ventilation with a facemask during elective/semi-elective endotracheal
intubation during their NICU admission.
Clinician resuscitators: Medical officers will be eligible to participate if they fulfill all the following criteria:
i. Employed at the study site
ii. Neonatology Staff Specialist/Neonatal Fellow/neonatal registrar (with minimum 6 months NICU experience)
iii. Successfully attend resuscitation training with the NEMO resuscitation monitor.
Neonates will be excluded from the study if they meet the following exclusion criteria:
i.Born with a potentially lethal congenital abnormality.
ii.Acute, severe, fetal compromise indicating intrapartum still birth (e.g., cessation of fetal heart rate).
iii.Unavailability of independent senior resuscitator.
iv.Unavailability of research team.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method