Automated Oxygen Control in Preterms on Non-invasive Ventilation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age22-34
SponsorKing's College Hospital NHS Trust

About this trial

This randomised controlled trial aims to investigate the effectiveness of closed-loop automated oxygen control (CLAC) in preterm infants receiving non-invasive respiratory support and determine if it reduces the duration of supplementary oxygen treatment and improves achievement of oxygen saturation targets, reduces the incidences of hypoxia and hyperoxia, the number of manual adjustments to the inspired oxygen concentration (FiO2), and adverse outcomes including bronchopulmonary dysplasia (BPD).

The study will take place at King's College Hospital neonatal intensive care unit (NICU). Parents of preterm infants born at less than 34 weeks of gestation and receiving non-invasive respiratory support will be approached, informed and if appropriate consented to join the trial.

Participants will be randomised to receiving either automated or manual oxygen control.

The study will measure outcomes including the duration of supplementary oxygen treatment, the percentage of time spent within oxygen saturation targets, the incidences of hypoxia and hyperoxia, the number of manual FiO2 adjustments required, the overall duration of non-invasive respiratory support and length of neonatal unit stay, and the incidence of BPD at 36 weeks postmenstrual age (PMA). Results will be compared between the two groups.

Eligibility criteria

Qualifiers

non-invasive positive pressure ventilation (NIPPV)

nasal CPAP

HHFNC oxygen, either as primary or post extubation respiratory support.

Disqualifiers

Infants with congenital cyanotic heart disease.

Infants with other know major congenital abnormalities.

Trial design

Treatments tested in this trial

  • Closed loop automated oxygen control

Treatment groups

76 Participants
are divided into 2 treatment groups