Conservative Versus Liberal Oxygenation Targets in Critically Ill Children (Oxy-PICU)
Primary Purpose
Critical Care, Hypoxia, Pediatric ALL
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Conservative oxygenation target
Liberal oxygenation target
Sponsored by
About this trial
This is an interventional treatment trial for Critical Care
Eligibility Criteria
Inclusion Criteria:
- less than 16 years and > 38 weeks corrected gestational age
- receiving supplemental oxygen for abnormal gas exchange
- emergency admission accepted to a participating paediatric intensive care unit (PICU) requiring mechanical ventilation within first 6 hours of face-to-face contact with PICU staff or transport team
Exclusion Criteria:
- recruited to Oxy-PICU in a previous admission
- brain pathology/injury as a primary reason for admission (e.g traumatic brain injury, post-cardiac arrest, stroke, convulsive status epilepticus without aspiration)
- known pulmonary hypertension
- known or suspected sickle cell disease
- known or suspected uncorrected congenital cardiac disease
- End-of-life care plan in place with limitation of resuscitation
- not expected to survive PICU admission
- receiving long-term mechanical ventilation prior to this admission (non-invasive ventilation or invasive ventilation)
Sites / Locations
- Great Ormond Street Hospital for Children
- St Mary's Hospital
- Southampton General Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Conservative oxygenation target
Liberal oxygenation target
Arm Description
Children in the conservative oxygenation target group receive treatment targeting oxygen saturation values of 88-92%.
Children in the liberal oxygenation target group receive treatment targeting oxygen saturation values of >94%.
Outcomes
Primary Outcome Measures
Number of eligible patients recruited per site per month
Secondary Outcome Measures
Proportion of parents/legal representatives refusing deferred consent
Proportion of eligible patients randomised
Distribution of time to randomisation
Proportion of systemic oxygen saturations within the target range in each group
Proportion of patients in each arm requiring other treatments influencing tissue oxygen delivery (blood transfusion, inotropic support)
Length of ventilation - proportion of randomised patients with outcome available in each group
Length of ventilation - mean (standard deviation) in each group
Length of ventilation - median and quartiles in each group.
Observed adverse events
Time taken for data collection and entry
Measurement of ischemia-modified albumin (plasma)
Measurement of malondialdehyde (plasma)
Measurement of total antioxidant status (plasma)
Length of PICU stay - proportion of randomised patients with outcome available in each group
Length of PICU stay - mean (standard deviation) in each group.
Length of PICU stay - median and quartiles in each group.
Hospital mortality - proportion of randomised patients with outcome available in each group
Hospital mortality - number (percentage) in each group.
PICU mortality - proportion of randomised patients with outcome available in each group
PICU mortality - number (percentage) in each group.
Days of organ specific support - proportion of randomised patients with outcome available in each group
Days of organ specific support - mean (standard deviation) in each group
Days of organ specific support - median and quartiles in each group
Measurement of hypoxia-inducible factor-1 alpha mRNA expression (leukocytes)
Full Information
NCT ID
NCT03040570
First Posted
November 21, 2016
Last Updated
February 22, 2018
Sponsor
Great Ormond Street Hospital for Children NHS Foundation Trust
Collaborators
Intensive Care National Audit & Research Centre, University of Southampton, St Mary's Hospital, London, University Hospital Southampton NHS Foundation Trust, University College, London
1. Study Identification
Unique Protocol Identification Number
NCT03040570
Brief Title
Conservative Versus Liberal Oxygenation Targets in Critically Ill Children
Acronym
Oxy-PICU
Official Title
A Randomised Pilot Multiple Centre Trial of Conservative Versus Liberal Oxygenation Targets in Critically Ill Children
Study Type
Interventional
2. Study Status
Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
March 4, 2017 (Actual)
Primary Completion Date
June 25, 2017 (Actual)
Study Completion Date
July 1, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Great Ormond Street Hospital for Children NHS Foundation Trust
Collaborators
Intensive Care National Audit & Research Centre, University of Southampton, St Mary's Hospital, London, University Hospital Southampton NHS Foundation Trust, University 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
A feasibility study to determine if it is possible to perform a safe, adequately powered, and affordable multi-centre study in critically ill children comparing current practice of liberal targets for systemic oxygen levels with more conservative targets.
Detailed Description
Around 19,000 critically ill children are admitted to paediatric intensive care units (PICU) each year in the UK. A large number of these children need breathing support, and this is usually provided through an invasive machine called a 'ventilator'. Clinicians make decisions for treatment based on how much oxygen their patient has in their blood (this is called oxygen saturation or oxygenation) and currently the amount of oxygen critically ill children need is not fully understood. This means that some clinicians use a lower oxygen saturation target, and others, a higher target. This may be problematic as research in neonates (babies) and adults has shown that oxygen saturation levels can influence a patient's chance of survival, how long they stay in hospital and healthcare costs.
Response to oxygen is different in babies, children and adults. This means that the results from the neonatal and adult research are unlikely to be valid or applicable in children due to age-related differences. Urgent high quality clinical evidence is therefore needed to inform on the best targets of oxygenation during critical illness in children.
As large clinical trials are expensive to conduct, it is important to demonstrate that a large-scale trial can be done and that the different components of a trial can all work together. Therefore, the Oxy-PICU study is a 'pilot randomised clinical trial' (a smaller version of the trial we would like to conduct) and will test the feasibility and safety of conducting a large scale trial comparing a restrictive oxygen saturation target (88-92%) with a more liberal oxygen saturation target (>94%). Oxy-PICU will also collect blood and urine samples to allow for in depth study of the biology of the different oxygenation targets.
The pilot trial will take place at three PICUs (two in London and one in Southampton) and aims to include between 115-125 eligible children over six months. Given the emergency nature of these children and the need to provide immediate care, informed consent will be sought after the children are entered into the study (this is known as deferred consent).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Care, Hypoxia, Pediatric ALL
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Conservative oxygenation target
Arm Type
Experimental
Arm Description
Children in the conservative oxygenation target group receive treatment targeting oxygen saturation values of 88-92%.
Arm Title
Liberal oxygenation target
Arm Type
Active Comparator
Arm Description
Children in the liberal oxygenation target group receive treatment targeting oxygen saturation values of >94%.
Intervention Type
Procedure
Intervention Name(s)
Conservative oxygenation target
Intervention Description
Participants allocated to the conservative oxygenation target group will receive supplemental oxygen and ventilator settings at the discretion of the treating clinical team with the aim of peripheral oxygen saturations remaining 88-92% (inclusive).
Intervention Type
Procedure
Intervention Name(s)
Liberal oxygenation target
Intervention Description
Participants allocated to the liberal oxygenation target group will receive supplemental oxygen and ventilator settings at the discretion of the treating clinical team with the aim of peripheral oxygen saturations remaining >94%.
Primary Outcome Measure Information:
Title
Number of eligible patients recruited per site per month
Time Frame
Baseline
Secondary Outcome Measure Information:
Title
Proportion of parents/legal representatives refusing deferred consent
Time Frame
Through study completion, an average of 24 hours
Title
Proportion of eligible patients randomised
Time Frame
Baseline
Title
Distribution of time to randomisation
Time Frame
Baseline
Title
Proportion of systemic oxygen saturations within the target range in each group
Time Frame
Through study completion, an average of 72 hours
Title
Proportion of patients in each arm requiring other treatments influencing tissue oxygen delivery (blood transfusion, inotropic support)
Time Frame
Through study completion, an average of 72 hours
Title
Length of ventilation - proportion of randomised patients with outcome available in each group
Time Frame
Through study completion, an average of 2 days
Title
Length of ventilation - mean (standard deviation) in each group
Time Frame
Through study completion, an average of 2 days
Title
Length of ventilation - median and quartiles in each group.
Time Frame
Through study completion, an average of 2 days
Title
Observed adverse events
Time Frame
28 days
Title
Time taken for data collection and entry
Time Frame
28 days
Title
Measurement of ischemia-modified albumin (plasma)
Time Frame
72 hours
Title
Measurement of malondialdehyde (plasma)
Time Frame
72 hours
Title
Measurement of total antioxidant status (plasma)
Time Frame
72 hours
Title
Length of PICU stay - proportion of randomised patients with outcome available in each group
Time Frame
Through study completion, an average of 2 days
Title
Length of PICU stay - mean (standard deviation) in each group.
Time Frame
Through study completion, an average of 2 days
Title
Length of PICU stay - median and quartiles in each group.
Time Frame
Through study completion, an average of 2 days
Title
Hospital mortality - proportion of randomised patients with outcome available in each group
Time Frame
Through study completion, an average of 2 days
Title
Hospital mortality - number (percentage) in each group.
Time Frame
Through study completion, an average of 2 days
Title
PICU mortality - proportion of randomised patients with outcome available in each group
Time Frame
Through study completion, an average of 2 days
Title
PICU mortality - number (percentage) in each group.
Time Frame
Through study completion, an average of 2 days
Title
Days of organ specific support - proportion of randomised patients with outcome available in each group
Time Frame
Through study completion, an average of 2 days
Title
Days of organ specific support - mean (standard deviation) in each group
Time Frame
Through study completion, an average of 2 days
Title
Days of organ specific support - median and quartiles in each group
Time Frame
Through study completion, an average of 2 days
Title
Measurement of hypoxia-inducible factor-1 alpha mRNA expression (leukocytes)
Time Frame
72 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
39 Weeks
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
less than 16 years and > 38 weeks corrected gestational age
receiving supplemental oxygen for abnormal gas exchange
emergency admission accepted to a participating paediatric intensive care unit (PICU) requiring mechanical ventilation within first 6 hours of face-to-face contact with PICU staff or transport team
Exclusion Criteria:
recruited to Oxy-PICU in a previous admission
brain pathology/injury as a primary reason for admission (e.g traumatic brain injury, post-cardiac arrest, stroke, convulsive status epilepticus without aspiration)
known pulmonary hypertension
known or suspected sickle cell disease
known or suspected uncorrected congenital cardiac disease
End-of-life care plan in place with limitation of resuscitation
not expected to survive PICU admission
receiving long-term mechanical ventilation prior to this admission (non-invasive ventilation or invasive ventilation)
Facility Information:
Facility Name
Great Ormond Street Hospital for Children
City
London
Country
United Kingdom
Facility Name
St Mary's Hospital
City
London
Country
United Kingdom
Facility Name
Southampton General Hospital
City
Southampton
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
29868973
Citation
Peters MJ, Jones GAL, Wiley D, Wulff J, Ramnarayan P, Ray S, Inwald D, Grocott M, Griksaitis M, Pappachan J, O'Neill L, Eaton S, Mouncey PR, Harrison DA, Rowan KM; Oxy-PICU Investigators for the Paediatric Intensive Care Society Study Group (PICS-SG). Conservative versus liberal oxygenation targets in critically ill children: the randomised multiple-centre pilot Oxy-PICU trial. Intensive Care Med. 2018 Aug;44(8):1240-1248. doi: 10.1007/s00134-018-5232-7. Epub 2018 Jun 4.
Results Reference
derived
PubMed Identifier
29247112
Citation
Jones GAL, Ramnarayan P, Raman S, Inwald D, Grocott MPW, Eaton S, Ray S, Griksaitis MJ, Pappachan J, Wiley D, Mouncey PR, Wulff J, Harrison DA, Rowan KM, Peters MJ; Oxy-PICU Investigators for thePaediatric Intensive Care Society-Study Group (PICS-SG). Protocol for a randomised pilot multiple centre trial of conservative versus liberal oxygenation targets in critically ill children (Oxy-PICU). BMJ Open. 2017 Dec 14;7(12):e019253. doi: 10.1136/bmjopen-2017-019253.
Results Reference
derived
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Conservative Versus Liberal Oxygenation Targets in Critically Ill Children
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