Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12609000764235
Ethics application status
Approved
Date submitted
27/08/2009
Date registered
3/09/2009
Date last updated
11/10/2017
Type of registration
Prospectively registered

Titles & IDs
Public title
The prophylactic hypothermia trial to lessen traumatic brain injury – randomised controlled trial.
Scientific title
Multi-centre randomised trial to evaluate the effect of early hypothermia on neurological function in patients with severe traumatic brain injury.
Secondary ID [1] 291677 0
NCT00987688
Universal Trial Number (UTN)
Trial acronym
POLAR-RCT
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Severe traumatic brain injury 243599 0
Condition category
Condition code
Neurological 239884 239884 0 0
Other neurological disorders
Injuries and Accidents 239885 239885 0 0
Other injuries and accidents

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Early and sustained hypothermia. Hypothermia will initially be induced by infusion of up to 2L ice cold saline. Following a safety assessment the patient will be rapidly cooled to 33C using surface temperature control equipment. They will be maintained at 33C for 72hours. Slow rewarming will occur at a rate of 1C/4hrs and will be titrated to intracranial pressure (ICP) control and blood pressure.
Intervention code [1] 241187 0
Treatment: Other
Comparator / control treatment
Standard management patients will be kept at normothermia (37C +/- 0.5C). If they develop a fever >38C they will be treated with paracetamol and surface temperature control equipment will be applied to maintain normothermia for up to 96 hours post randomisation. After 96 hours post randomisation Standard care patients will be managed as per unit protocol. Cooling to 35C is an option for refractory ICP.
Control group
Active

Outcomes
Primary outcome [1] 240670 0
The proportion of favourable neurological outcomes (Glasgow Outcome Score Extended: GOSE 5 to 8)
Timepoint [1] 240670 0
6 months post injury
Secondary outcome [1] 257306 0
Quality of life assessments
*SF-12 (version 1)
*EQ5D
Timepoint [1] 257306 0
6 months post injury
Secondary outcome [2] 257307 0
Mortality
Timepoint [2] 257307 0
6 months post injury, hospital discharge & Intensive Care Unit (ICU)discharge
Secondary outcome [3] 257308 0
Proportion of favourable (GOSE 5-8) neurological outcomes in survivors
Timepoint [3] 257308 0
6 months post injury
Secondary outcome [4] 257309 0
Incidence of adverse events
*Significant bleeding - assessed clinically
*Infection - assessed clinically
Timepoint [4] 257309 0
Assessed as part of normal intensive care management during the study intervention
Secondary outcome [5] 257766 0
Cumulative proportion of patients with Acute Kidney Injury (Injury/Failure Risk Injury Failure Loss End stage (RIFLE) categories) in those receiving cooling v. normothermia
Timepoint [5] 257766 0
Day 7 of hospital admission.
Secondary outcome [6] 257767 0
Levels of biomarkers neutrophil gelatinase-associated lipocalin (NGAL), cystatin C and liver-type fatty acid binding protein (L-FABP) will be measured in plasma and urine from blood and urine specimens obtained from 50 patients. Levels of these biomarkers will be compared in those receiving cooling v. normothermia. Urine NGAL will be measured using the Abbott point-of-care test and other measurements will be performed in accredited laboratories using standardised methods for each biomarker.
Timepoint [6] 257767 0
24hrs, 48 hrs, 72 hrs post Intensive Care admission

Eligibility
Key inclusion criteria
Pre-hospital Inclusion Criteria
*Blunt trauma with clinical diagnosis of severe Traumatic Brain Injury (TBI) and Glasgow Coma Scale <9
*Estimated age = 18 and < 60 years of age
*The patient is intubated or intubation is imminent
Emergency Dept Inclusion Criteria
*Blunt trauma with clinical diagnosis of severe TBI and GCS <9
*Estimated age > or = 18 and < 60 years of age
*The patient is intubated or intubation is imminent
Minimum age
18 Years
Maximum age
60 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
***********Pre-hospital Exclusion Criteria
Clinical diagnosis of drug or alcohol intoxication as predominant cause of coma
Randomisation unable to be performed within 3 hrs of estimated time of injury
Estimated transport time to study hospital >2.5hrs
Able to be intubated without drugs
Systolic BP <90mmHg
Heart rate > 120bpm
Cardiac arrest at the scene or in transit
GCS=3 and un-reactive pupils
Penetrating neck/torso injury
Known or obvious pregnancy
Receiving hospital is not a study site
Evidence of current anti-coagulant treatment
Known to be carer dependent due to a pre-existing neurological condition

***********Emergency Dept Exclusion Criteria
Clinical diagnosis of drug or alcohol intoxication as predominant cause of coma
Randomisation unable to be performed within 3 hrs of estimated time of injury
Able to be intubated without drugs
Persistent Systolic BP <90mmHg
GCS=3 + un-reactive pupils
Cardiac arrest at the scene or in transit
Clinically significant bleeding likely to require haemostatic intervention, for example:
Bleeding into the chest, abdomen or retro-peritoneum likely to require surgery +/- embolisation
**Pelvic fracture likely to require surgery +/- embolisation
**More than two long bone fractures requiring operative fixation
**Penetrating neck/torso injury
Positive urine or blood pregnancy test
Evidence of current anti-coagulant treatment
Known to be carer dependent due to a pre-existing neurological condition
In the treating clinician’s opinion, “cooling” is not in the patient’s best interest

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Sealed opaque envelope/randomisation
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
The random allocation sequence will be generated by a computer program. randomisation will be in variable block sizes. Randomisation will be stratified by ambulance base and hospital.
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Outcome assessor blinded to treatment allocation
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
1/04/2010
Actual
20/04/2010
Date of last participant enrolment
Anticipated
1/10/2017
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
500
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
QLD,WA,VIC
Recruitment hospital [1] 7824 0
The Alfred - Prahran
Recruitment hospital [2] 7825 0
Royal Melbourne Hospital - Royal Park campus - Parkville
Recruitment hospital [3] 7826 0
Princess Alexandra Hospital - Woolloongabba
Recruitment hospital [4] 7827 0
Royal Perth Hospital - Perth
Recruitment hospital [5] 7828 0
Sir Charles Gairdner Hospital - Nedlands
Recruitment hospital [6] 7829 0
Gold Coast University Hospital - Southport
Recruitment postcode(s) [1] 15766 0
4215 - Southport
Recruitment outside Australia
Country [1] 1962 0
New Zealand
State/province [1] 1962 0
Auckland
Country [2] 8792 0
France
State/province [2] 8792 0
Country [3] 8793 0
Switzerland
State/province [3] 8793 0
BERN
Country [4] 8794 0
Qatar
State/province [4] 8794 0
Doha

Funding & Sponsors
Funding source category [1] 237541 0
Government body
Name [1] 237541 0
NHMRC
Country [1] 237541 0
Australia
Funding source category [2] 237542 0
Charities/Societies/Foundations
Name [2] 237542 0
Victorian Neurotrauma Initiative
Country [2] 237542 0
Australia
Primary sponsor type
University
Name
Australian and New Zealand Intensive Care-Research Centre, Monash University
Address
Level 3 Burnet building
89 Commercial Rd
Melbourne
Vic, 3004
Country
Australia
Secondary sponsor category [1] 237022 0
None
Name [1] 237022 0
Address [1] 237022 0
Country [1] 237022 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 243680 0
The Alfred Human Research & Ethics Committee
Ethics committee address [1] 243680 0
Ethics committee country [1] 243680 0
Australia
Date submitted for ethics approval [1] 243680 0
16/04/2009
Approval date [1] 243680 0
28/05/2009
Ethics approval number [1] 243680 0
HREC number 154-09

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 30093 0
Prof David 'Jamie' Cooper
Address 30093 0
Australian and New Zealand Intensive Care - Research Centre
School of Public Health and Preventive Medicine
The Department of Epidemiology and Preventive Medicine
Monash University
Level 3, 553 St Kilda Road
Melbourne Vic, 3004
Country 30093 0
Australia
Phone 30093 0
+61 3 99030343
Fax 30093 0
Email 30093 0
[email protected]
Contact person for public queries
Name 13340 0
MS Lynne Murray
Address 13340 0
ANZIC-RC
Monash University
Level 3 Burnet Building
89 Commercial Rd
Melbourne
Vic, 3004
Country 13340 0
Australia
Phone 13340 0
+61 3 99030513
Fax 13340 0
+61 3 99030071
Email 13340 0
[email protected]
Contact person for scientific queries
Name 4268 0
Prof Jamie Cooper
Address 4268 0
ANZIC-RC
Monash University
Level 3 Burnet Building
89 Commercial Rd
Melbourne
Vic, 3004
Country 4268 0
Australia
Phone 4268 0
+61 3 90762838
Fax 4268 0
+61 3 99030071
Email 4268 0
[email protected]

No information has been provided regarding IPD availability


What supporting documents are/will be available?

Current supporting documents:


Updated to:
Doc. No.TypeCitationLinkEmailOther DetailsAttachment
23157Other   
23158OtherTerms of reference / data sharing policyhttps://www.monash.edu/__data/assets/pdf_file/0008/1852316/2019-07-23-ANZIC-RC-Terms-of-Ref.pdf 
23159Statistical analysis plan   
23160Informed consent form   
23161Clinical study report   
23799Other    al documents can be requested through the custodia... [More Details]

Results publications and other study-related documents

Documents added manually
Current Study Results
No documents have been uploaded by study researchers.

Update to Study Results
Doc. No.TypeIs Peer Reviewed?DOICitations or Other DetailsAttachment
4265Study results articleYes 308414-(Uploaded-16-09-2019-16-11-07)-Journal results publication.pdf

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseStatistical analysis plan for the POLAR-RCT: The Prophylactic hypOthermia trial to Lessen trAumatic bRain injury-Randomised Controlled Trial.2018https://dx.doi.org/10.1186/s13063-018-2610-y
EmbaseMeasured energy expenditure in mildly hypothermic critically ill patients with traumatic brain injury: A sub-study of a randomized controlled trial.2021https://dx.doi.org/10.1016/j.clnu.2021.05.012
N.B. These documents automatically identified may not have been verified by the study sponsor.