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Effects of Closed-loop Automatic Control of FiO2 in Extremely Preterm Infants (FiO2-C)

U

University Hospital Tuebingen

Status and phase

Active, not recruiting
Phase 3

Conditions

Infant,Premature

Treatments

Device: closed-loop automatic control of the inspiratory fraction of oxygen (FiO2-C)

Study type

Interventional

Funder types

Other

Identifiers

NCT03168516
2018-000453-41 (EudraCT Number)
FiO2-C
BMBF-Fz01KG1602 (Other Grant/Funding Number)

Details and patient eligibility

About

Extremely low gestational age neonates (ELGANs), i.e. those born at <28 weeks, frequently experience intermittent hypoxemic/hyperoxemic episodes. Observational data indicate that severe and prolonged hypoxemic episodes are associated with retinopathy of prematurity (ROP), impaired long-term development and death. Closed-loop automated control of the inspiratory fraction of oxygen (FiO2-C) reduces time outside the oxygen target range, decreases number and duration of hypo- and hyperoxemic episodes, and reduces caregivers' workload. The proposed observer-blinded randomized controlled trial was designed and will be powered to compare the effect of FiO2-C in addition to manual adjustments, in comparison with manual adjustments of FiO2 only, on death and severe complications of prematurity thought to be related to hypoxia/hyperoxia and neurodevelopmental impairment in ELGANs. The results of this trial may help to improve the quality of life of ELGANs and reduce the burden of significant morbidity as well as costs for health care and society

Full description

Approximately 0.5% of all neonates (i.e., about 25,000 infants per year in Europe) are extremely low gestational age neonates (ELGANs), i.e. have a gestational age (GA) of <28 completed weeks at birth. ELGANs have higher incidences of mortality, retinopathy of prematurity (ROP), chronic lung disease and other risks of prematurity as well as severe neurodevelopmental impairment.

The vast majority of ELGANs require supplemental oxygen in addition to mechanical respiratory support (including CPAP). Irrespective of the SpO2 target, the vast majority of ELGANs suffers from recurrent intermittent hypoxemic and (as a consequence of inappropriate adjustments of FiO2) hyperoxemic episodes. Recurrent intermittent hypoxic episodes - i.e. wide fluctuations in oxygen levels - are associated with an increased risk of ROP and there are data that suggest that late deaths and neurodevelopmental impairment are also linked to them.

Continuous positive airway pressure (CPAP) has been shown to reduce extubation failure in preterm infants, which may in part be due to a reduced frequency and severity of apnea of prematurity and stabilized functional residual capacity during apnea. Keeping oxygen levels (i.e., SpO2) stable despite irregular breathing patterns in ELGANs, requires frequent adjustments of the FiO2 which is both challenging, time consuming, and often impossible due to limited personnel resources.

FiO2-Controllers have been developed by several manufacturers of infant ventilators. They reduce the burden of hyper-/hypoxemia in infants while being safe and accurate in very short-term studies. The effects of FiO2-C on clinically relevant outcome measures and the safety of long-term continuous application, however, have yet to be elucidated. Hence there is now a window of opportunity to assess this new technology for benefits and harms, before it is implemented into neonatal care without appropriate evaluation of its safety and efficacy.

Enrollment

1,065 patients

Sex

All

Ages

Under 48 hours old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Preterm infants with a gestational age (GA) at birth of 23+0/7 - 27+6/7 weeks

Exclusion criteria

  • Decision for palliative care
  • congenital anomalies
  • postnatal age > 48h
  • missing parental consent
  • lack of device enabling closed-loop automatic control of FiO2

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,065 participants in 2 patient groups

Experimental intervention
Experimental group
Description:
closed-loop automatic control of the inspiratory fraction of oxygen (FiO2-C)
Treatment:
Device: closed-loop automatic control of the inspiratory fraction of oxygen (FiO2-C)
Control intervention
No Intervention group
Description:
Standard care, i.e. manual adjustments of the FiO2 only

Trial contacts and locations

32

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Central trial contact

Christian Maiwald, Dr.; Center for pediatric clinical trials (CPCS) Tuebingen

Data sourced from clinicaltrials.gov

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