Automated Versus Manual Control Of Oxygen For Preterm Infants On Continuous Positive Airway Pressure In Nigeria
- Conditions
- Neonatal Respiratory Distress Related ConditionsNeonatal Respiratory FailureOxygen ToxicityPrematurity
- Registration Number
- NCT05508308
- Lead Sponsor
- Murdoch Childrens Research Institute
- Brief Summary
One in ten babies are born preterm (\<37 weeks gestation) globally. Complications of prematurity are the leading cause of death in children under 5 years, with the highest mortality rate in Sub-Saharan Africa (SSA). Low flow oxygen, and respiratory support - where an oxygen/air mixture is delivered under pressure - are life saving therapies for these babies. Bubble Continuous Positive Airway Pressure (bCPAP) is the mainstay of neonatal respiratory support in SSA.
Oxygen in excess can damage the immature eyes (Retinopathy of Prematurity \[ROP\]) and lungs (Chronic Lung Disease) of preterm babies. Historically, in well-resourced settings, excessive oxygen administration to newborns has been associated with 'epidemics' of ROP associated blindness. Today, with increasing survival of preterm babies in SSA, and increasing access to oxygen and bCPAP, there are concerns about an emerging epidemic of ROP. Manually adjusting the amount of oxygen provided to an infant on bCPAP is difficult, and fearing the risks of hypoxaemia (low oxygen levels) busy health workers often accept hyperoxaemia (excessive oxygen levels). Some well resourced neonatal intensive care units globally have adopted Automated Oxygen Control (AOC), where a computer uses a baby's oxygen saturation by pulse oximetry (SpO2) to frequently adjust how much oxygen is provided, targetting a safe SpO2 range. This technology has never been tested in SSA, or partnered with bCPAP devices that would be more appropriate for SSA.
This study aims to compare AOC coupled with a low cost and robust bCPAP device (Diamedica Baby CPAP) - OxyMate - with manual control of oxygen for preterm babies on bCPAP in two hospitals in south west Nigeria. The hypothesis is that OxyMate can significantly and safely increase the proportion of time preterm infants on bCPAP spend in safe oxygen saturation levels.
- Detailed Description
Trial description: A randomised cross-over trial of manual versus automated control of oxygen (OxyMate) for preterm infants on bCPAP. This trial will use an established technology (automated oxygen titration algorithm, VDL1.1) partnered with a low-cost bCPAP device in a low-resource setting. It will involve preterm infants requiring bCPAP respiratory support with allocation to OxyMate or manual oxygen control for consecutive 24 h periods in random sequence.
Objectives: This trial seeks to examine safety and potential efficacy of our automated oxygen configuration (OxyMate) in preterm infants in a setting characterised by financial constraints, workforce limitations, and underdeveloped infrastructure, and assess contextual feasibility and appropriateness to inform future definitive clinical trials and product development.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 49
- <34 weeks gestation (or birth weight < 2kg if gestation not known)
- ≥12 hours old
- Receiving CPAP support and supplemental oxygen (FiO2 >0.21) for respiratory insufficiency
- Projected requirement for CPAP and oxygen therapy for > 48 hours
- Deemed likely to fail CPAP in the next 48 hours
- Deemed clinically unstable or recommended for palliation by treating team
- Cause of hypoxaemia likely to be non-respiratory - e.g. cyanotic heart disease
- Informed consent from parent/guardians not obtained
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Proportion of time in target SpO2 range Measured for each 24 hour study epoch Proportion of time (over total recorded time) in the target SpO2 range (91-95%, or 91-100% when in room air). Measured as %time
- Secondary Outcome Measures
Name Time Method Length of stay Up to 4 weeks post enrollment Measured in days
Proportion of time in severe hypoxaemia Measured for each 24 hour study epoch Proportion of time (over total recorded time) with SpO2 \<80% (severe hypoxaemia). Measured as %time
Costs Measured at completion of OxyMate study: an estimated 20 weeks Total costs of prototype system (Diamedica +/- Automated Oxygen control - OxyMate)
Proportion of time in target SpO2 range when receiving supplemental oxygen Measured for each 24 hour study epoch Proportion of time (over total recorded time) in SpO2 target range (91-95%) when receiving supplemental oxygen. Measured as %time when receiving oxygen
Proportion of time in hypoxaemia Measured for each 24 hour study epoch Proportion of time (over total recorded time) with SpO2\<90% (hypoxaemia). Measured as %time
No response to prolonged severe hypoxaemia (frequency) Measured for each 24 hour study epoch Number of periods of no FiO2 increment for ≥30 seconds with SpO2 \<80% (i.e. failure to respond to severe hypoxaemia). Measured as episodes per hour
Time on low flow oxygen Completed for each participant at end of their study period: 49 hours from study commencement Duration of time on low-flow oxygen therapy. Measured in hours
Frequency of prolonged hypoxaemia episodes Measured for each 24 hour study epoch Frequency of 30 seconds episodes with SpO2 continuously \<80% (severe hypoxaemic episodes). Measured as episodes per hour
Proportion of time in hyperoxaemia Measured for each 24 hour study epoch Proportion of time (over total recorded time) with SpO2 \>96% when receiving supplemental oxygen (hyperoxaemia). Measured as %time when receiving oxygen
Severe hypoxaemia with bradycardia (frequency) Measured for each 24 hour study epoch Number of periods with SpO2 \<80% for ≥30 seconds with any bradycardia (heart rate \<100 bpm). Measured as episodes per hour
Acceptability and usability Completed for each participant (health workers) at end of an infant's study period (49 hours). Results recorded for unique health workers through to OxyMate study completion: estimated 20 weeks Mean/median user acceptability score (total and per question) on Likert scale from structured questionnaire. Scores range from 1 (strongly disagree) to 5 (strongly agree) with posed statement or question
Duration of CPAP and oxygen therapy Completed for each participant at end of their study period: 49 hours from study commencement Duration of time on CPAP with supplemental oxygen. Measured in hours
Final discharge outcome Up to 4 weeks post enrollment Measured as categorical outcome (died in hospital, discharged well, discharged against medical advice, other)
Device malfunction Measured through to OxyMate study completion: estimated 20 weeks Number of OxyMate malfunction events
CPAP in room air Completed for each participant at end of their study period: 49 hours from study commencement Duration of time on CPAP in room air. Measured in hours
Proportion of time in severe hyperoxaemia Measured for each 24 hour study epoch Proportion of time (over total recorded time) with SpO2 \>98% when receiving supplemental oxygen (severe hyperoxaemia). Measured as %time when receiving oxygen
Frequency of prolonged hyperoxaemia episodes Measured for each 24 hour study epoch Frequency of 30 seconds episodes with SpO2 continuously \>96% (hyperoxaemic episodes). Measured as episodes per hour
Manual FiO2 adjustments Measured for each 24 hour study epoch Frequency of manual FiO2 adjustments. Measured as FiO2 adjustments/hour
No response to prolonged severe hypoxaemia (duration) Measured for each 24 hour study epoch Duration of periods of no FiO2 increment for ≥30 seconds with SpO2 \<80% (i.e. failure to respond to severe hypoxaemia). Measured as mean duration per episode
Severe hypoxaemia with bradycardia (duration) Measured for each 24 hour study epoch Duration of periods with SpO2 \<80% for ≥30 seconds with any bradycardia (heart rate \<100 bpm). Measured as mean duration per episode
Trial Locations
- Locations (2)
Sacred Heart Hospital
🇳🇬Lantoro, Abeokuta, Nigeria
University College Hospital
🇳🇬Agodi, Ibadan, Nigeria
Sacred Heart Hospital🇳🇬Lantoro, Abeokuta, Nigeria