search
Back to results

Optimising Neonatal Ventilation With Closed-loop Oxygen Control

Primary Purpose

Infant, Newborn, Diseases, Mechanical Ventilation Complication

Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Closed-loop automated oxygen control (Oxygenie, SLE6000)
Sponsored by
King's College Hospital NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Infant, Newborn, Diseases

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Infants born at or above 34 weeks completed gestation requiring mechanical ventilation and admitted to King's NICU within 24 hours of initiation of mechanical ventilation. Exclusion Criteria: Preterm infants less than 34 weeks gestation Infants with cyanotic congenital heart disease Infants on high frequency oscillatory ventilation (HFOV)

Sites / Locations

  • King's College HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Other

Arm Label

Manual oxygen control

Closed-loop automated oxygen control (Oxygenie, SLE 6000)

Arm Description

Standard ventilation with inspired oxygen concentration adjusted manually as per unit's protocol.

Ventilation with Oxygenie software (closed-loop automated oxygen control system), adjusted by clinical staff as necessary

Outcomes

Primary Outcome Measures

The duration of oxygen treatment
The duration of oxygen treatment will be measured in median (interquartile range) number of days of oxygen treatment for participants in each group.
The percentage of time spent in hyperoxia
Target oxygen saturation range for our study population is 92-96%. Hyperoxia is defined as the time spent with oxygen saturation levels exceeding 96%. The time spent in hyperoxia will be calculated as a percentage of the total time of monitoring.

Secondary Outcome Measures

The percentage of time spent receiving an inspired oxygen concentration (FiO2) above 30%
The time spent with an FiO2>30% will be calculated as a percentage of the total time of monitoring.

Full Information

First Posted
December 12, 2022
Last Updated
December 12, 2022
Sponsor
King's College Hospital NHS Trust
Collaborators
King's College London
search

1. Study Identification

Unique Protocol Identification Number
NCT05657795
Brief Title
Optimising Neonatal Ventilation With Closed-loop Oxygen Control
Official Title
Does Closed-loop Automated Oxygen Control During Mechanical Ventilation Reduce the Duration of Supplementary Oxygen Treatment and the Amount of Time Spent in Hyperoxia? A Randomised Trial in Ventilated Infants Born at or Near Term
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 7, 2022 (Actual)
Primary Completion Date
December 1, 2023 (Anticipated)
Study Completion Date
December 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
King's College Hospital NHS Trust
Collaborators
King's College London

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Ventilated newborns frequently need supplemental oxygen but its use must be monitored carefully as both giving too much or too little oxygen can have harmful effects. Giving too little oxygen results to low oxygen levels (hypoxia) and increases the risk of complications and mortality. Excessive oxygen delivery (hyperoxia) increases the risk of diseases involving several organs such as the retinas and the lungs. Although infants born very preterm require support with their breathing more often, more mature neonates may also need to be ventilated at birth and to receive supplemental oxygen. Therefore, they may suffer from problems related to hypoxia and hyperoxia. For the above reasons, oxygen levels are continuously monitored and the amount of oxygen provided is manually adjusted by the nurses and doctors. Closed-loop automated oxygen control systems (CLAC) are a more recent approach that involves the use of a computer software added to the ventilator. This software allows for automatic adjustment of the amount of oxygen provided to the baby in order to maintain oxygen levels within a desired target range depending on the baby's age and clinical condition. Previous studies in preterm and very small infants showed that automated oxygen control systems provided the right amount of oxygen for most of the time and prevented hypoxia and hyperoxia with fewer manual adjustments required by clinical staff. Preliminary results from a study that included infants born at 34 weeks gestation and beyond showed that CLAC systems allowed to reduce the amount of supplementary oxygen more rapidly. With this study we aim to compare the time spent in hyperoxia and the overall duration of oxygen treatment between infants whose oxygen is adjusted either manually or automatically while they remain ventilated. This will help us understand if CLAC systems help reduce the complications related to oxygen treatment.
Detailed Description
This will be a randomised controlled trial. The investigators aim to recruit a minimum of forty ventilated infants born at or above 34 weeks of gestation. Participants will be randomised to either closed-loop automated oxygen control or manually controlled oxygen from recruitment to successful extubation. Informed written consent will be requested from the parents or legal guardians of the infants and the attending neonatal consultant will be requested to assent to the study. Eligible infants whose parents consent to the study will be enrolled within 24 hours of initiation of mechanical ventilation. Randomisation will be performed using an online randomisation generator. Patients will be ventilated using SLE6000 ventilators. Ventilator settings will be manually adjusted by the clinical team as per unit's protocol. The intervention group, in addition to standard care will also be connected to the Oxygenie closed-loop oxygen saturation monitoring software (SLE). This software uses oxygen saturations from the SpO2 probe attached to the neonate, fed into an algorithm, to automatically adjust the percentage of inspired oxygen to maintain oxygen saturations within the target range. Manual adjustments to the inspired oxygen concentration will be allowed at any point during the study if deemed appropriate by the clinical team. Patient will be studied from enrolment till successful extubation. If an infant fails extubation and required reintubation within 48 hours, he will be studied in his initial study arm. Therefore, for the infants randomised at the intervention group CLAC will resume.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infant, Newborn, Diseases, Mechanical Ventilation Complication

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participating infants will be randomised either to manual oxygen control or closed-loop automated oxygen control, adjusted by clinical staff as necessary.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Manual oxygen control
Arm Type
No Intervention
Arm Description
Standard ventilation with inspired oxygen concentration adjusted manually as per unit's protocol.
Arm Title
Closed-loop automated oxygen control (Oxygenie, SLE 6000)
Arm Type
Other
Arm Description
Ventilation with Oxygenie software (closed-loop automated oxygen control system), adjusted by clinical staff as necessary
Intervention Type
Device
Intervention Name(s)
Closed-loop automated oxygen control (Oxygenie, SLE6000)
Intervention Description
The OxyGenie closed-loop oxygen saturation monitoring software (SLE) uses oxygen saturations from the SpO2 probe attached to the neonate, fed into an algorithm, to automatically adjust the percentage of inspired oxygen to maintain oxygen saturations within the target range. Manual adjustments including the percentage of FiO2 will be allowed at any point during the study if deemed appropriate by the clinical team.
Primary Outcome Measure Information:
Title
The duration of oxygen treatment
Description
The duration of oxygen treatment will be measured in median (interquartile range) number of days of oxygen treatment for participants in each group.
Time Frame
Through study completion, an average of 1 year
Title
The percentage of time spent in hyperoxia
Description
Target oxygen saturation range for our study population is 92-96%. Hyperoxia is defined as the time spent with oxygen saturation levels exceeding 96%. The time spent in hyperoxia will be calculated as a percentage of the total time of monitoring.
Time Frame
Through study completion, an average of 1 year
Secondary Outcome Measure Information:
Title
The percentage of time spent receiving an inspired oxygen concentration (FiO2) above 30%
Description
The time spent with an FiO2>30% will be calculated as a percentage of the total time of monitoring.
Time Frame
Through study completion, an average of 1 year

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants born at or above 34 weeks completed gestation requiring mechanical ventilation and admitted to King's NICU within 24 hours of initiation of mechanical ventilation. Exclusion Criteria: Preterm infants less than 34 weeks gestation Infants with cyanotic congenital heart disease Infants on high frequency oscillatory ventilation (HFOV)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ourania Kaltsogianni, MSc
Phone
(+44)02032999000
Ext
38492
Email
ourania.kaltsogianni@nhs.net
First Name & Middle Initial & Last Name or Official Title & Degree
Anne Greenough, Professor
Email
anne.greenough@kcl.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Theodore Dassios, PhD
Organizational Affiliation
King's College Hospital/ King's College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
King's College Hospital
City
London
ZIP/Postal Code
SE5 9RS
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ourania Kaltsogianni, MSc
Phone
02032999000
Ext
38492
Email
ourania.kaltsogianni@nhs.net

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21833494
Citation
Ramadan G, Paul N, Morton M, Peacock JL, Greenough A. Outcome of ventilated infants born at term without major congenital abnormalities. Eur J Pediatr. 2012 Feb;171(2):331-6. doi: 10.1007/s00431-011-1549-8. Epub 2011 Aug 11.
Results Reference
background
PubMed Identifier
30287066
Citation
Williams LZJ, McNamara D, Alsweiler JM. Intermittent Hypoxemia in Infants Born Late Preterm: A Prospective Cohort Observational Study. J Pediatr. 2019 Jan;204:89-95.e1. doi: 10.1016/j.jpeds.2018.08.048. Epub 2018 Oct 1.
Results Reference
background
PubMed Identifier
27225960
Citation
Lakshminrusimha S, Konduri GG, Steinhorn RH. Considerations in the management of hypoxemic respiratory failure and persistent pulmonary hypertension in term and late preterm neonates. J Perinatol. 2016 Jun;36 Suppl 2:S12-9. doi: 10.1038/jp.2016.44.
Results Reference
background
PubMed Identifier
32732378
Citation
Salverda HH, Cramer SJE, Witlox RSGM, Dargaville PA, Te Pas AB. Automated oxygen control in preterm infants, how does it work and what to expect: a narrative review. Arch Dis Child Fetal Neonatal Ed. 2021 Mar;106(2):215-221. doi: 10.1136/archdischild-2020-318918. Epub 2020 Jul 30.
Results Reference
background
PubMed Identifier
32969040
Citation
Sturrock S, Ambulkar H, Williams EE, Sweeney S, Bednarczuk NF, Dassios T, Greenough A. A randomised crossover trial of closed loop automated oxygen control in preterm, ventilated infants. Acta Paediatr. 2021 Mar;110(3):833-837. doi: 10.1111/apa.15585. Epub 2020 Oct 6.
Results Reference
background
PubMed Identifier
33832390
Citation
Abdo M, Hanbal A, Asla MM, Ishqair A, Alfar M, Elnaiem W, Ragab KM, Nourelden AZ, Zaazouee MS. Automated versus manual oxygen control in preterm infants receiving respiratory support: a systematic review and meta-analysis. J Matern Fetal Neonatal Med. 2022 Dec;35(25):6069-6076. doi: 10.1080/14767058.2021.1904875. Epub 2021 Apr 8.
Results Reference
background

Learn more about this trial

Optimising Neonatal Ventilation With Closed-loop Oxygen Control

We'll reach out to this number within 24 hrs