Trial Review

Registering a new trial?

To achieve prospective registration, we recommend submitting your trial for registration at the same time as ethics submission.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12612000513819
Ethics application status
Approved
Date submitted
14/05/2012
Date registered
14/05/2012
Date last updated
6/09/2016
Type of registration
Prospectively registered

Titles & IDs
Public title
Permissive HyperthErmiA Through Avoidance of Paracetamol in Known or Suspected Infection in the Intensive Care Unit (ICU)
Scientific title
A phase 2b randomised controlled trial investigating the safety and efficacy of intravenous paracetamol versus placebo (5% dextrose) in the treatment of fever in critically ill patients with known or suspected infection.
Secondary ID [1] 280481 0
Nil
Universal Trial Number (UTN)
Trial acronym
The HEAT trial
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Known or suspected infection in critically ill patients in the Intensive Care Unit (ICU) 286461 0
Condition category
Condition code
Infection 286718 286718 0 0
Studies of infection and infectious agents

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
This study follows on from a previous pilot study with a similar design (http://www.anzctr.org.au/ACTRN12611000981921.aspx) After randomisation, the patient will receive paracetamol (1gm intravenously) or placebo 6 hourly until one of the following occurs:
1. the patient ceases antimicrobial therapy
2. the patient is discharged from ICU
3. the patient is deemed to have completed the course of study medication (as described below)
4. the patient reaches day 28 post randomisation (672 hours post randomisation)

Provided that the patient remains on antimicrobial therapy and remains in ICU, they will receive paracetamol or placebo until at least the morning of study day 2. On the morning of study day 2 at 8 am the patient will be assessed. If the patient has not had a standardised body temperature of less than 37.5 degrees celsius for the previous 24 hours, they will continue to receive paracetamol or placebo 6 hourly and will be assessed by the research co-ordinator on each subsequent morning to determine if they have had a standardised body temperature of less than 37.5 degrees celsius for the previous 24 hours. If, at the time of assessment, the patient has had a standardised body temperature of less than 37.5 degrees celsius for the entire past 24 hours, further study treatment will be withheld. If the patient does not develop a fever of greater than or equal to 38 degrees celsius within 48 hours, they will be deemed to have completed the course of study medication. If the patient does develop another standardised body temperature of greater than or equal to 38 degrees celsius, the patient will restart study medication and, thereafter, they will be assessed each morning at 8 am to determine whether they a have had a standardised body temperature of less than 37.5 degrees celsius for a period of 24 hours at which point medication will be withheld and then stopped as described above.

Once the patient has completed the course of study medication, they may receive open label paracetamol at the discretion of the treating clinician.
Intervention code [1] 284847 0
Treatment: Drugs
Comparator / control treatment
100ml 5% dextrose intravenously 6 hourly until one of the four conditions stated above in the Description of intervention(s) / exposure field occurs
Control group
Placebo

Outcomes
Primary outcome [1] 287115 0
The primary efficacy measure is the number of "alive ICU-free days" to study day 28. The number of ICU-free days will be calculated as 28 minus the number of days in ICU (excluding days of ICU readmission). Patients who die before day 90 will be counted as having zero ICU free days.
Timepoint [1] 287115 0
ICU-free survival will be determined at 672 hours from the time of randomisation
Secondary outcome [1] 297402 0
Mean daily temperature measured via axillary thermometer
Timepoint [1] 297402 0
Study day 0 to day 7 while in ICU (determined from 6 hourly temperature measurements at 00:00hr, 06:00hr, 12:00hr, and 18:00hr)
Secondary outcome [2] 297403 0
Maximum daily temperature via axillary thermometer
Timepoint [2] 297403 0
Maximum daily temperature recorded at any time during the calendar day each day from day 0 to day 28 while the patient is in ICU
Secondary outcome [3] 297404 0
Proportion of subjects who stop study treatment due to the development of liver dysfunction (defined as development of a serum bilirubin of greater than twice the upper limit of normal or a serum aspartate aminotransferase (AST) / serum alanine aminotransferase (ALT) of greater than five times the upper limit of normal.)

Note that only one of AST or ALT is required to be measured with the choice depending on local hospital preference.
Timepoint [3] 297404 0
Bilirubin and AST / ALT are mandatory for day 0 to day 7 while the subject is in ICU
Secondary outcome [4] 297405 0
Incidence of creatinine kinase >5000 (serum assay)
Timepoint [4] 297405 0
Study day 0, 3, 5 and 7
Secondary outcome [5] 297406 0
Delta creatinine (difference between pre-randomisation creatinine and the highest creatinine recorded during the first seven days in ICU)
Timepoint [5] 297406 0
Daily for study day 0 to day 7
Secondary outcome [6] 297407 0
ICU-support-free survival. The number of ICU-support-free survival days will be calculated as 28 minus the number of days in ICU (excluding days of ICU readmission) that the patient received any of the following supports - invasive ventilation, non-invasive ventilation, inotrope or vasopressor support, renal replacement therapy or other extracorporeal support. Patients who die before day 90 will be counted as having zero ICU free days.
Timepoint [6] 297407 0
day 28. The number of hours of each type of ICU support will be recorded daily.
Secondary outcome [7] 297408 0
Hospital-free survival. The number of hospital-free days survival days will be calculated as 28 minus the number of days in hospital (excluding days of hospital readmission). This will be determined from the hospital discharge date documented in the medical record. Patients who die before day 90 will be counted as having zero ICU free days.
Timepoint [7] 297408 0
day 28
Secondary outcome [8] 297409 0
Mechanical ventilation free survival will be calculated as 28 minus the number of days in ICU receiving mechanical ventilation (excluding days of ICU readmission). This will be determined from the medical record. Patients who die before day 90 will be counted as having zero ICU free days.
Timepoint [8] 297409 0
day 28. The number of hours of mechanical ventilation will be recorded daily until day 28 to allow calculation of this end point
Secondary outcome [9] 297410 0
Inotrope / vasopressor free survival will be calculated as 28 minus the number of days in ICU receiving inotropes or vasopressors (excluding days of ICU readmission). This will be determined from the medical record. Patients who die before day 90 will be counted as having zero ICU free days.
Timepoint [9] 297410 0
day 28. The number of hours of inotrope / vasopressor support will be recorded daily until day 28 to allow calculation of this end point
Secondary outcome [10] 297411 0
ICU length of stay reported for survivors and non survivors separately determined from the medical record
Timepoint [10] 297411 0
Censored at day 90
Secondary outcome [11] 297412 0
Hospital length of stay reported for survivors and non survivors separately determined from the medical record
Timepoint [11] 297412 0
Censored at day 90
Secondary outcome [12] 297413 0
C reactive protein (serum assay) performed in local hospital laboratories and determined from examination of the medical record.
Timepoint [12] 297413 0
study day 0, 3, 5, and 7 for patients who remain in ICU
Secondary outcome [13] 297414 0
mean arterial pressure measured invasively (where performed invasively via an arterial and non-invasively when invasive measures measurements are not available). Measurements as recorded in the ICU flow chart (i.e. medical record)
Timepoint [13] 297414 0
6 hourly until study day 3; daily for study days 4-7 for patients who remain in ICU
Secondary outcome [14] 297415 0
heart rate as documented in the ICU flow chart (i.e. medical record)
Timepoint [14] 297415 0
6 hourly until study day 3; daily for study days 4-7 for patients who remain in ICU
Secondary outcome [15] 297416 0
minute ventilation (for mechanically ventilated patients only) a recorded on the ICU flow chart (i.e. medical record)
Timepoint [15] 297416 0
6 hourly until study day 3; daily for study days 4-7 for patients who remain in ICU
Secondary outcome [16] 297418 0
mortality determined by phone follow-up
Timepoint [16] 297418 0
day 28
Secondary outcome [17] 297419 0
mortality determined by phone follow-up
Timepoint [17] 297419 0
day 90

Eligibility
Key inclusion criteria
Patients are eligible to be included in the study only if they meet the following criteria at the time of randomisation:
1. Age greater than or equal to16 years
2. Standardised body temperature greater than or equal to 38.0 degrees within the previous 12 hours.
3. Receiving antimicrobial therapy for a known or suspected infection (this does NOT include post-operative patients who are receiving antibiotics for the purposes of prophylaxis rather than treatment)
Minimum age
16 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Patients will be excluded from the study if they meet ANY of the following criteria:
1. AST or ALT greater than five times the upper limit of normal OR bilirubin greater than twice the upper limit of normal OR any other contraindication to 4gm paracetamol per day
2. a requirement for ongoing NSAID use (in excess of low dose aspirin);
3. evidence of acute brain injury during the current hospital admission (defined as any acute traumatic brain injury, subarachnoid haemorrhage, acute ischaemic stroke, acute intracerebral haemorrhage, or acute intracranial infection); hyperthermic syndromes (including heat stroke; current biochemical evidence of thyrotoxicosis (thyroid function tests are not required prior to recruitment into the trial unless clinically indicated); malignant hyperthermia, neuroleptic malignant syndrome, or other drug-induced hyperthermia)
4. admission to ICU following a cardiac arrest which is currently being treated with therapeutic hypothermia;
5. there is a limitation of therapy order or aggressive treatment is deemed unsuitable
6. patients who are moribund and, in whom, death is perceived to be imminent (within 24 hours);
7. any patient with rhabdomyolysis that is deemed by the treating clinician to be clinically significant.
8. any patient transferred from another ICU who fulfilled all inclusion criteria in the other ICU and spent >12 hours in the other ICU prior to transfer
9. any patient who is pregnant;
10. previously randomised into the HEAT trial or previously eligible for enrolment during the current ICU admission but not enrolled in the study (i.e. patients who were not enrolled within 12 hours of onset of fever in association with satisfying other eligibility criteria may not be enrolled at a later point in the ICU admission)

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)
Randomisation and treatment allocation will be achieved by a web-based randomisation and drug allocation system via password-protected encrypted website interface. All staff and patients will be blinded as to the treatment allocation. Treatment will be allocated in boxes of 12 bottles of study medication (maximum of 3 days supply) and resupply will be performed via a web-based system
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Block randomisation stratified by centre using computer generated random numbers, generated by the study statistician.
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Multicentred study
Phase
Phase 2 / Phase 3
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
1/11/2012
Actual
20/03/2013
Date of last participant enrolment
Anticipated
30/06/2014
Actual
29/07/2014
Date of last data collection
Anticipated
Actual
1/11/2015
Sample size
Target
700
Accrual to date
Final
700
Recruitment in Australia
Recruitment state(s)
ACT,NSW,VIC
Recruitment outside Australia
Country [1] 4301 0
New Zealand
State/province [1] 4301 0

Funding & Sponsors
Funding source category [1] 285239 0
Government body
Name [1] 285239 0
Health Research Council of New Zealand
Country [1] 285239 0
New Zealand
Primary sponsor type
Charities/Societies/Foundations
Name
Medical Research Institute of New Zealand
Address
Private Bag 7902
Wellington 6242

Level 7, CSB Building
Wellington Hospital
Riddiford St, Newtown
Wellington 6021
New Zealand
Country
New Zealand
Secondary sponsor category [1] 284104 0
Other Collaborative groups
Name [1] 284104 0
Australian and New Zealand Intensive Care Society Clinical Trials Group
Address [1] 284104 0
PO Box 164
Carlton South
Victoria 3053
Country [1] 284104 0
Australia
Other collaborator category [1] 260798 0
Charities/Societies/Foundations
Name [1] 260798 0
The George Institute for Global Health
Address [1] 260798 0
Level 7, 341 George St, Sydney NSW 2000 Australia. Postal Address: PO Box M201, Missenden Rd, NSW 2050 Australia.
Country [1] 260798 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 287247 0
Multiregion Ethics Committee of the Health Research Council of New Zealand
Ethics committee address [1] 287247 0
c/- Ministry of Health
PO Box 5013
1 The Terrace
Wellington 6011
Ethics committee country [1] 287247 0
New Zealand
Date submitted for ethics approval [1] 287247 0
Approval date [1] 287247 0
26/05/2011
Ethics approval number [1] 287247 0
MEC/11/01/004

Summary
Brief summary
Fever is an adaptive response to infections which occurs widely in the animal kingdom. The suppression of fever increases the risk of mortality in animals, although the effect of antipyretics in critically ill patients is unknown. The objective of this study is to determine whether paracetamol influences the risk of mortality in critically ill patients with fever and known or suspected infection. A phase 2b double blind randomised placebo controlled trial of paracetamol will be undertaken in 700 patients with fever and known or suspected infection in New Zealand and Australia under the auspices of the Australian and New Zealand Intensive Care Society Clinical Trials Group (ANZICS CTG). If either the aggressive or permissive antipyretic regimes influence outcomes including survival in patients with fever and infection, the findings will have a major impact on the burden of infectious disease in New Zealand and internationally.

Pilot study registered at http://www.anzctr.org.au/ACTRN12611000981921.aspx
Trial website
www.heat-trial.org.nz
Trial related presentations / publications
Young P, Saxena M, Bellomo R, Freebairn R, Hammond N, van Haren F, Holliday M,
Henderson S, Mackle D, McArthur C, McGuinness S, Myburgh J, Weatherall M, Webb S,
Beasley R; HEAT Investigators; Australian and New Zealand Intensive Care Society
Clinical Trials Group. Acetaminophen for Fever in Critically Ill Patients with
Suspected Infection. N Engl J Med. 2015 Dec 3;373(23):2215-24. doi:
10.1056/NEJMoa1508375.
Public notes

Contacts
Principal investigator
Name 34172 0
Dr Paul Young
Address 34172 0
Intensive Care Unit Wellington Regional Hospital Private Bag 7902 Riddiford Street Newtown 6021 Wellington
Country 34172 0
New Zealand
Phone 34172 0
+64274552269
Fax 34172 0
Email 34172 0
[email protected]
Contact person for public queries
Name 17419 0
Paul Young
Address 17419 0
Intensive Care Unit
Wellington Regional Hospital
Private Bag 7902
Riddiford Street
Newtown 6021
Wellington
Country 17419 0
New Zealand
Phone 17419 0
+64 27 455 2269
Fax 17419 0
Email 17419 0
[email protected]
Contact person for scientific queries
Name 8347 0
Paul Young
Address 8347 0
Intensive Care Unit
Wellington Regional Hospital
Private Bag 7902
Riddiford Street
Newtown 6021
Wellington
Country 8347 0
New Zealand
Phone 8347 0
+64 27 455 2269
Fax 8347 0
Email 8347 0
[email protected]

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

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

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseAcetaminophen for fever in critically III patients with suspected infection.2015https://dx.doi.org/10.1056/NEJMoa1508375
N.B. These documents automatically identified may not have been verified by the study sponsor.