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Trial registered on ANZCTR


Registration number
ACTRN12613000303741
Ethics application status
Approved
Date submitted
18/03/2013
Date registered
19/03/2013
Date last updated
2/03/2021
Date data sharing statement initially provided
2/03/2021
Date results provided
2/03/2021
Type of registration
Prospectively registered

Titles & IDs
Public title
High Flow Nasal Cannulae as Primary Support in the Treatment of Early Respiratory Distress (The HIPSTER Trial)
Scientific title
A multi-centre, randomised, controlled, non-inferiority trial comparing high flow nasal cannulae to nasal continuous positive airway pressure as primary respiratory support, in preterm infants of 28 weeks' gestation and above, with early respiratory distress or apnoea, assessing assigned treatment failure within 72 hours.
Secondary ID [1] 282139 0
nil
Universal Trial Number (UTN)
Trial acronym
The HIPSTER Trial
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Respiratory distress of the newborn 288639 0
Condition category
Condition code
Respiratory 288979 288979 0 0
Other respiratory disorders / diseases
Reproductive Health and Childbirth 288980 288980 0 0
Complications of newborn

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
High flow nasal cannula (HFNC) therapy. Heated, humidified, blended gas (air/oxygen) will be delivered at a flow rate of 4-8 L/minute using either Fisher & Paykel or Vapotherm circuits and nasal prongs. HFNC prong size will be selected as per the manufacturer's recommendations (maintaining a leak at the nares) and there will be no alterations to the manufacturer's recommended set-up of the circuit.

1. Infants randomised to HFNC will commence on flow rates of 6-8 L/min.

2. HFNC limits will be 4-8 L/min from trial entry until discharge home.

3. The attending clinical team will increase/decrease flow rates at their discretion in whole number flow increments (e.g. 4, 5, 6, 7, 8 L/min) and these changes will require a documented medical order. Infants should be reviewed at least every 24 hours and weaning considered if they are clinically improving with FiO2 (fraction of inspired oxygen) <0.30.

4. The flow rate should not exceed 8 L/min in any infant.

5. Infants who are stable on HFNC at 4 L/min, with FiO2 <0.30, for more than 24 hours, may cease HFNC and be tried in air or on low flow nasal cannulae (cessation at this stage is not mandatory; earlier cessation will be at the discretion of the attending clinical team if FiO2 <0.30).

6. Infants who satisfy failure criteria whilst receiving HFNC at 8 L/min will cease HFNC and receive ‘rescue’ NCPAP initially at 7-8 cm H2O (physician discretion). These infants will be deemed to have treatment failure for the primary outcome. Infants who subsequently again satisfy the failure criteria on NCPAP of 8 cm H2O, still within the primary outcome period of 72 hours, will be intubated and mechanically ventilated.

7. Should the decision be taken to recommence non-invasive respiratory support later during their admission (including post-extubation), infants in the HFNC group should again initially receive HFNC, unless they previously experienced treatment failure with HFNC. They may subsequently receive NCPAP at the discretion of the attending clinical team.
Intervention code [1] 286747 0
Treatment: Devices
Comparator / control treatment
Nasal continuous positive airway pressure (NCPAP). This is defined as the use of short binasal prongs to deliver humidified, blended gas (air/oxygen) with any NCPAP device (including ventilator-generated or ‘bubble’ NCPAP).

1. Infants randomised to NCPAP will commence on pressures of 6-8 cm H2O.

2. NCPAP pressure limits are 5-8 cm H2O during the primary outcome period. After this point set NCPAP pressures are at the discretion of the attending clinician.

3. Changes to NCPAP pressures will be made at the discretion of the attending clinical team, with a documented medical order for any change.

4. Infants randomised to NCPAP will not receive HFNC for 72 hours after trial entry. After this period, HFNC should still not be used unless an infant has moderate to severe nasal trauma, defined as at least three consecutive scores of 2, or any score of 3 or more, on the Trial Nasal Trauma Chart.

5. The attending clinical team will increase or decrease NCPAP pressures at their discretion in whole number increments (e.g. 5, 6, 7, 8 cm H2O), and these changes will require a documented medical order. Infants should be reviewed at least every 24 hours and weaning considered if they are clinically improving with FiO2 <0.30

6. Infants who are stable on NCPAP at 5 cm H2O, with FiO2 <0.30, for more than 24 hours, may cease NCPAP and be tried in air or on low flow nasal cannulae (cessation at this stage is not mandatory; earlier cessation will be at the discretion of the attending clinical team if FiO2 <0.30).

7. Infants who satisfy failure criteria whilst receiving NCPAP 8 cm H2O will be intubated and mechanically ventilated. These infants will be deemed to have treatment failure for the primary outcome.

8. Should the decision be taken to recommence non-invasive respiratory support later during the admission (including post-extubation), infants in the NCPAP group should again receive NCPAP, unless they have already suffered moderate to severe nasal trauma from NCPAP as described above.
Control group
Active

Outcomes
Primary outcome [1] 289099 0
The primary outcome is treatment failure within 72 hours after initiation of the assigned treatment. To fail the assigned treatment, the infant must be receiving maximal therapy (NCPAP 8 cm H2O or HFNC 8 L/min), plus at least one of:

- Sustained fraction of inspired oxygen (FiO2) requirement 0.40 or more to maintain peripheral oxygen saturation (SpO2) within the specified normal limits of the participating centre
- pH 7.20 or lower and pCO2 >60 mm Hg on free-flowing capillary or arterial blood gas sample, taken at least 1 hour after initiation of assigned treatment
- Six or more apnoeas requiring intervention (not self-resolving) within any 6-hour period, or 2 or more apnoeas requiring positive pressure ventilation within any 24-hour period

Treatment failure will also be adjudged to have occurred in any infant requiring urgent intubation and mechanical ventilation (at medical discretion)
Timepoint [1] 289099 0
72 hours after initiation of allocated treatment.
Secondary outcome [1] 301790 0
Treatment failure in the pre-defined gestational age subgroups (less than 32 weeks, and 32 weeks and above)
Timepoint [1] 301790 0
72 hours after intitiation of allocated treatment
Secondary outcome [2] 301791 0
Reason for commencing non-invasive respiratory support, which may include one or more of:
- Clinical signs of respiratory distress (tachypnea >60 breaths/minute, audible grunting, intercostal/subcostal recession)
- Oxygen requirement
- Respiratory acidosis on blood gas sampling
- Apnoea
Timepoint [2] 301791 0
At initiation of allocated treatment
Secondary outcome [3] 301792 0
Reason(s) for treatment failure if applicable (number of infants who failed for each defined criteria)
Timepoint [3] 301792 0
72 hours after initiation of allocated treatment
Secondary outcome [4] 301793 0
Incidence of intubation and mechanical ventilation within the 72 hour primary outcome period, and at any time during the hospital admission; overall and within GA subgroups
Timepoint [4] 301793 0
At discharge from hospital
Secondary outcome [5] 301794 0
Incidence of bronchopulmonary dysplasia (BPD), defined as a supplemental oxygen requirement and/or receiving respiratory support at 36 weeks’ post-menstrual age (PMA)
Timepoint [5] 301794 0
At 36 weeks' post-menstrual age
Secondary outcome [6] 301795 0
Incidence of pneumothorax or other air leak (e.g. pneumomediastinum, pulmonary interstitial emphysema) while receiving the assigned treatment, and at any point from trial entry until hospital discharge
Timepoint [6] 301795 0
At hospital discharge
Secondary outcome [7] 301796 0
Total number of days of any respiratory support, and total number of days of each type of respiratory support (including HFNC, NCPAP, non-synchronised nasal intermittent positive pressure ventilation [nsNIPPV] and mechanical ventilation via an endotracheal tube) received after trial entry until discharge from hospital, with one day defined as a calendar day where a treatment was received for any time period (thus some days may be counted for more than one type of support)
Timepoint [7] 301796 0
At hospital discharge
Secondary outcome [8] 301797 0
Last day of supplemental oxygen received, recorded as day of life and also as PMA at final cessation of oxygen
Timepoint [8] 301797 0
At hospital discharge
Secondary outcome [9] 301798 0
Number of infants discharged home with oxygen
Timepoint [9] 301798 0
At hospital discharge
Secondary outcome [10] 301799 0
Number of infants treated with postnatal corticosteroids for lung disease
Timepoint [10] 301799 0
At hospital discharge
Secondary outcome [11] 301800 0
Incidence of significant neonatal morbidities after trial entry until discharge from hospital:
Confirmed sepsis, including
- Septicaemia, defined as any positive blood culture and treatment with IV antibiotics for at least 48 hours
- Meningitis, defined as growth of a single organism from cerebrospinal fluid (CSF) and/or a raised CSF white cell count
(Note that during a single illness episode, an infant may satisfy criteria for more than one of the above)
Patent ductus arteriosus treated with medication and/or surgery
Necrotising enterocolitis (NEC) Bell’s stage 2 or above
Isolated intestinal perforation (not associated with NEC)
Incidence of the following diagnoses on any cranial ultrasound
- Intraventricular haemorrhage grade III or IV
- Cystic periventricular leukomalacia
- Post-haemorrhagic ventricular dilatation and whether it required intervention
Retinopathy of prematurity requiring laser eye surgery in one or both eyes
Timepoint [11] 301800 0
At hospital discharge
Secondary outcome [12] 301801 0
Duration of caffeine therapy in days, and PMA at cessation
Timepoint [12] 301801 0
At hospital discharge
Secondary outcome [13] 301802 0
Number of days to reach full feeds, defined as tolerating at least 120 ml/kg/day of milk, or demand suck feeding (breast or bottle) with no intravenous fluids.
Timepoint [13] 301802 0
At hospital discharge
Secondary outcome [14] 301803 0
Number of days to reach full suck feeds, defined as the first day on which no intravenous fluids or nasogastric/orogastric feeds are given
Timepoint [14] 301803 0
At hospital discharge
Secondary outcome [15] 301805 0
Proportion of infants fully breast-fed at discharge home from hospital
Timepoint [15] 301805 0
At hospital discharge
Secondary outcome [16] 301807 0
Weight gain, calculated as:
Last weight (g) before discharge home from hospital minus birth weight (g), giving a weight gain in g/day from birth to discharge
Timepoint [16] 301807 0
At hospital discharge
Secondary outcome [17] 301812 0
Incidence of nasal trauma stage 2 or above as recorded on the Trial Nasal Trauma Chart, the type of respiratory support the infant was receiving at the time of the first such recorded trauma, and whether a change to the type of respiratory support was required (The same scoring system will be used in all participating centres)
Timepoint [17] 301812 0
At hospital discharge
Secondary outcome [18] 301813 0
Duration of hospital admission, including
- Days in any level III (tertiary) hospital, and
- Total number of days in any hospital
Timepoint [18] 301813 0
At hospital discharge
Secondary outcome [19] 301814 0
Incidence of transfer to another hospital prior to first discharge home
Timepoint [19] 301814 0
At hospital discharge
Secondary outcome [20] 301815 0
Proportion of infants who die before discharge
Timepoint [20] 301815 0
At hospital discharge

Eligibility
Key inclusion criteria
1. Preterm infants of at least 28 weeks and <37 weeks’ GA at birth by best obstetric estimate
2. Age <24 hours
3. Admitted to the neonatal intensive care unit (NICU) of a participating centre, whether inborn or outborn
4. Prospective parental consent obtained
5. Decision has been made, at or after admission to the NICU, by the attending clinician, to commence or continue non-invasive respiratory support (some infants may have received a brief period of NCPAP prior to admission to the NICU, as part of their standard care during resuscitation/stabilisation at delivery and/or during transfer from the birth centre or theatre)
6. At randomisation, infant has received <4 hours NCPAP support
7. Full intensive care is being offered
Minimum age
No limit
Maximum age
24 Hours
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. GA <28 weeks, or 37 weeks and above, at birth
2. Previous intubation and mechanical ventilation, or immediate need for intubation and mechanical ventilation, as determined by the attending clinician
3. Any infant who is receiving NCPAP 8 cm H2O and already satisfying the treatment failure criteria, as specified above
4. Any infant who has received 4 hours or more of NCPAP support
5. Participation in a concurrent study that prohibits inclusion in this trial
6. Known major upper airway, lower respiratory tract, cardiac or gastrointestinal tract anomaly
7. Known air leak syndrome

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)
There will be pre-randomisation stratification by gestational age (<32 weeks’, and 32 weeks’ gestation and above) and by centre. Multiple births will be randomised individually. The trial statistician will provide sets of consecutively numbered, sealed opaque envelopes containing the assigned treatment, using varying block sizes. The envelope will be opened either prior to the infant arriving on the neonatal unit if he/she is already receiving non-invasive support, or immediately after the a decision has been made to commence or continue non-invasive support in an infant already admitted to the unit.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
The randomisation will be in randomly permuted blocks of variable length, stratified by study centre, and by gestational age.
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
27/05/2013
Actual
27/05/2013
Date of last participant enrolment
Anticipated
Actual
16/06/2015
Date of last data collection
Anticipated
Actual
31/12/2015
Sample size
Target
750
Accrual to date
Final
564
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 779 0
The Royal Women's Hospital - Parkville
Recruitment hospital [2] 4520 0
Royal Brisbane & Womens Hospital - Herston
Recruitment hospital [3] 4521 0
Mercy Hospital for Women - Heidelberg
Recruitment hospital [4] 4522 0
Monash Medical Centre - Clayton campus - Clayton
Recruitment postcode(s) [1] 6592 0
3052 - Parkville
Recruitment postcode(s) [2] 12120 0
4006 - Herston
Recruitment postcode(s) [3] 12121 0
3084 - Heidelberg
Recruitment postcode(s) [4] 12122 0
3168 - Clayton
Recruitment outside Australia
Country [1] 7279 0
Norway
State/province [1] 7279 0
East Norway, North Norway

Funding & Sponsors
Funding source category [1] 286909 0
Government body
Name [1] 286909 0
National Health and Medical Research Council
Country [1] 286909 0
Australia
Funding source category [2] 286910 0
Hospital
Name [2] 286910 0
The Royal Women's Hospital
Country [2] 286910 0
Australia
Primary sponsor type
Individual
Name
Professor Peter Davis
Address
The Royal Women's Hospital
Cnr Grattan Street & Flemington Road
Parkville
Victoria 3052
Country
Australia
Secondary sponsor category [1] 285697 0
None
Name [1] 285697 0
Address [1] 285697 0
Country [1] 285697 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 288968 0
The Royal Women's Hospital Human Research Ethics Committee
Ethics committee address [1] 288968 0
Ethics committee country [1] 288968 0
Australia
Date submitted for ethics approval [1] 288968 0
06/03/2013
Approval date [1] 288968 0
16/05/2013
Ethics approval number [1] 288968 0
EC00259
Ethics committee name [2] 290613 0
The Royal Children's Hospital Human Research Ethics Committee
Ethics committee address [2] 290613 0
Ethics committee country [2] 290613 0
Australia
Date submitted for ethics approval [2] 290613 0
05/08/2013
Approval date [2] 290613 0
22/08/2013
Ethics approval number [2] 290613 0
EC00238
Ethics committee name [3] 293765 0
Mercy Hospital for Women Human Research Ethics Committee
Ethics committee address [3] 293765 0
Ethics committee country [3] 293765 0
Australia
Date submitted for ethics approval [3] 293765 0
Approval date [3] 293765 0
27/11/2013
Ethics approval number [3] 293765 0
R13/34
Ethics committee name [4] 293766 0
South-Eastern Norway Regional Health Authority Research Ethics Committee
Ethics committee address [4] 293766 0
Ethics committee country [4] 293766 0
Norway
Date submitted for ethics approval [4] 293766 0
Approval date [4] 293766 0
01/01/2014
Ethics approval number [4] 293766 0
2013/1657

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

Contacts
Principal investigator
Name 38554 0
Dr Calum Roberts
Address 38554 0
Department of Newborn Research
Level 7
The Royal Women's Hospital
Cnr Grattan Street & Flemington Road
Parkville
Victoria 3052
Country 38554 0
Australia
Phone 38554 0
+61383453770
Fax 38554 0
+61383453789
Email 38554 0
[email protected]
Contact person for public queries
Name 38555 0
Calum Roberts
Address 38555 0
Department of Newborn Research
Level 7
The Royal Women's Hospital
Cnr Grattan Street & Flemington Road
Parkville
Victoria 3052
Country 38555 0
Australia
Phone 38555 0
+61383453770
Fax 38555 0
+61383453789
Email 38555 0
[email protected]
Contact person for scientific queries
Name 38556 0
Calum Roberts
Address 38556 0
Department of Newborn Research
Level 7
The Royal Women's Hospital
Cnr Grattan Street & Flemington Road
Parkville
Victoria 3052
Country 38556 0
Australia
Phone 38556 0
+61383453770
Fax 38556 0
+61383453789
Email 38556 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No/undecided IPD sharing reason/comment


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
EmbaseA multicentre, randomised controlled, non-inferiority trial, comparing High flow therapy with nasal continuous positive airway pressure as primary support for preterm infants with respiratory distress (the HIPSTER trial): Study protocol.2015https://dx.doi.org/10.1136/bmjopen-2015-008483
EmbaseHigh-flow nasal cannulae as primary respiratory support for preterm infants-an international, multi-centre, randomised, controlled, non-inferiority trial.2016https://dx.doi.org/10.1111/jpc.13194
EmbaseNasal high flowas primary respiratory support for preterm infants.2016https://dx.doi.org/10.1007/s00431-016-2785-8
EmbaseNasal high-flow therapy for primary respiratory support in preterm infants.2016https://dx.doi.org/10.1056/NEJMoa1603694
EmbaseCost-Effectiveness Analysis of Nasal Continuous Positive Airway Pressure Versus Nasal High Flow Therapy as Primary Support for Infants Born Preterm.2018https://dx.doi.org/10.1016/j.jpeds.2017.12.072
EmbaseRefining the Use of Nasal High-Flow Therapy as Primary Respiratory Support for Preterm Infants.2018https://dx.doi.org/10.1016/j.jpeds.2018.01.031
EmbasePredictors and Outcomes of Early Intubation in Infants Born at 28-36 Weeks of Gestation Receiving Noninvasive Respiratory Support.2020https://dx.doi.org/10.1016/j.jpeds.2019.09.026
N.B. These documents automatically identified may not have been verified by the study sponsor.