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Trial registered on ANZCTR
Registration number
ACTRN12613000202763
Ethics application status
Approved
Date submitted
19/02/2013
Date registered
19/02/2013
Date last updated
14/01/2021
Date data sharing statement initially provided
4/09/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
The Breathing for Life Trial: A randomised controlled trial of fractional exhaled nitric oxide based management of asthma during pregnancy and its impact on perinatal outcomes and infant and childhood respiratory health
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Scientific title
The Breathing for Life Trial: A multi-centre randomised controlled trial of fractional exhaled nitric oxide based management of asthma during pregnancy and its impact on perinatal outcomes and infant and childhood respiratory health.
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Secondary ID [1]
281396
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Nil
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Universal Trial Number (UTN)
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Trial acronym
BLT
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Asthma during pregnancy
287633
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Condition category
Condition code
Respiratory
287965
287965
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0
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Asthma
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Reproductive Health and Childbirth
287966
287966
0
0
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Antenatal care
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Reproductive Health and Childbirth
287967
287967
0
0
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Complications of newborn
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
FENO Algorithm: Fractional exhaled nitric oxide (FENO) is a non-invasive marker of airway inflammation in asthma. FENO will be measured at monthly visits during the second and third trimesters pregnancy and the level used to adjust maintenance asthma therapy. When FENO is high, inhaled corticosteroid therapy will be increased, when FENO is in a mid-range no change will be made to ICS, and when FENO is low, ICS will be decreased. If symptoms are present (assessed using the asthma control questionnaire), long acting beta agonist (LABA) will be added.
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Intervention code [1]
285875
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Other interventions
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Comparator / control treatment
Standardised Usual Care: Pregnant women will receive an initial asthma assessment, and asthma therapy (inhaled corticosteroid and long acting beta agonist) will be adjusted by their usual care providers. FENO measurements will not be made.
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Control group
Active
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Outcomes
Primary outcome [1]
288177
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Adverse perinatal outcome (either preterm birth [delivery <37 completed weeks gestation], intrauterine growth restriction [birth weight <10th centile], perinatal mortality [stillbirth or neonatal death within first 28 days of life] or neonatal hospitalisation at birth
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Assessment method [1]
288177
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Timepoint [1]
288177
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First 28 days of life
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Secondary outcome [1]
299546
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Preterm birth (delivery at <37 completed weeks gestation)
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Assessment method [1]
299546
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Timepoint [1]
299546
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Birth
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Secondary outcome [2]
299547
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Intrauterine growth restriction (Birth weight <10th centile)
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Assessment method [2]
299547
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Timepoint [2]
299547
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Birth
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Secondary outcome [3]
299548
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Perinatal mortality
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Assessment method [3]
299548
0
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Timepoint [3]
299548
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First 28 days of life
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Secondary outcome [4]
299549
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Neonatal hospitalisation at birth
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Assessment method [4]
299549
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Timepoint [4]
299549
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Birth
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Secondary outcome [5]
299550
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Maternal asthma exacerbations requiring medical intervention during pregnancy
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Assessment method [5]
299550
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Timepoint [5]
299550
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End of pregnancy
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Secondary outcome [6]
299551
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Maternal hospitalisations for asthma during pregnancy
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Assessment method [6]
299551
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Timepoint [6]
299551
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End of pregnancy
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Secondary outcome [7]
299552
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Multiple episodes of bronchiolitis in the first year of life, parent-report by the Questionnaire on respiratory symptoms in preschool children (Strippoli et al. Arch Dis Child. 2007), which has demonstrated test-retest reliability.
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Assessment method [7]
299552
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Timepoint [7]
299552
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12 months of age
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Secondary outcome [8]
299553
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Multiple episodes of croup in the first year of life, parent-report by the Questionnaire on respiratory symptoms in preschool children (Strippoli et al. Arch Dis Child. 2007), which has demonstrated test-retest reliability.
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Assessment method [8]
299553
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Timepoint [8]
299553
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12 months of age
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Secondary outcome [9]
300643
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Atopy at age 3
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Assessment method [9]
300643
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Timepoint [9]
300643
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3 years of age
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Secondary outcome [10]
300644
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Physician diagnosed asthma at age 6
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Assessment method [10]
300644
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Timepoint [10]
300644
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6 years of age
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Secondary outcome [11]
301011
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Mean birth weight
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Assessment method [11]
301011
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Timepoint [11]
301011
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Birth
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Secondary outcome [12]
301012
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Hospitalisation for bronchiolitis in first year of life
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Assessment method [12]
301012
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Timepoint [12]
301012
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12 months of age
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Secondary outcome [13]
301300
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Maternal hospitalisations or emergency department presentations for asthma during pregnancy
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Assessment method [13]
301300
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Timepoint [13]
301300
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End of pregnancy
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Secondary outcome [14]
301301
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Hospitalisation or emergency department presentation for severe respiratory illness (bronchiolitis, croup or wheezing) in the first year of life
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Assessment method [14]
301301
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Timepoint [14]
301301
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12 months of age
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Eligibility
Key inclusion criteria
12-22 weeks gestation
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Minimum age
18
Years
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Maximum age
50
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Inability to attend monthly study visits, inability to perform manoeuvres required for spirometry or FENO, drug or alcohol dependence, unknown dates, chronic oral steroid use or use of immunosuppressant therapy.
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation concealed by blinded randomisation list held by independent statistician
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated random number list stratified by study centre and maternal smoking
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people assessing the outcomes
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
5/03/2013
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Actual
7/03/2013
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Date of last participant enrolment
Anticipated
31/12/2019
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Actual
11/06/2019
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Date of last data collection
Anticipated
31/01/2020
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Actual
28/01/2020
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Sample size
Target
1200
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Accrual to date
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Final
1200
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,QLD
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Recruitment hospital [1]
409
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John Hunter Hospital Royal Newcastle Centre - New Lambton
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Recruitment hospital [2]
410
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The Maitland Hospital - Maitland
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Recruitment hospital [3]
411
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Royal North Shore Hospital - St Leonards
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Recruitment hospital [4]
412
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Nepean Hospital - Kingswood
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Recruitment hospital [5]
413
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Royal Brisbane & Womens Hospital - Herston
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Recruitment hospital [6]
414
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Royal Hospital for Women - Randwick
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Recruitment hospital [7]
6432
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The Canberra Hospital - Garran
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Recruitment postcode(s) [1]
5836
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2305
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Recruitment postcode(s) [2]
5837
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2320
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Recruitment postcode(s) [3]
5838
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2065
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Recruitment postcode(s) [4]
5839
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2747
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Recruitment postcode(s) [5]
5840
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4029
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Recruitment postcode(s) [6]
5841
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2031
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Recruitment postcode(s) [7]
13977
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2605 - Garran
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Funding & Sponsors
Funding source category [1]
286152
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Government body
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Name [1]
286152
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National Health and Medical Research Council (application ID 1060983)
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Address [1]
286152
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Level 1, 16 Marcus Clarke Street
Canberra ACT 2601
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Country [1]
286152
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Australia
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Primary sponsor type
Hospital
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Name
John Hunter Hospital (Hunter New England Local Health District)
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Address
Locked Bag 1,
HRMC
Newcastle NSW 2310
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Country
Australia
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Secondary sponsor category [1]
284960
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Individual
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Name [1]
284960
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Prof Peter Gibson
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Address [1]
284960
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Centre for Asthma and Respiratory Diseases
Level 2, West Wing,
Hunter Medical Research Institute
Locked Bag 1, HRMC
Newcastle NSW 2310
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Country [1]
284960
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Australia
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Other collaborator category [1]
277125
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University
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Name [1]
277125
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University of Newcastle
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Address [1]
277125
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University Drive
Callaghan NSW 2308
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Country [1]
277125
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Australia
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Other collaborator category [2]
277126
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Hospital
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Name [2]
277126
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The Maitland Hospital
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Address [2]
277126
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550-560 High Street
Maitland NSW 2320
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Country [2]
277126
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Australia
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Other collaborator category [3]
277127
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Hospital
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Name [3]
277127
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Royal Hospital for Women, Randwick
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Address [3]
277127
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Barker Street
Randwick NSW 2031
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Country [3]
277127
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Australia
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Other collaborator category [4]
277128
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Hospital
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Name [4]
277128
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Royal North Shore Hospital
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Address [4]
277128
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Pacific Highway
St Leonards NSW 2065
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Country [4]
277128
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Australia
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Other collaborator category [5]
277129
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Hospital
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Name [5]
277129
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Royal Brisbane and Women's Hospital
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Address [5]
277129
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Cnr Butterfield St and Bowen Bridge Rd
Herston Qld 4029
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Country [5]
277129
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Australia
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Other collaborator category [6]
277130
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Hospital
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Name [6]
277130
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Nepean Hospital
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Address [6]
277130
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Derby Street
Kingswood NSW 2747
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Country [6]
277130
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Australia
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Other collaborator category [7]
279155
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Hospital
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Name [7]
279155
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The Canberra Hospital
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Address [7]
279155
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Yamba Dr, Garran
ACT 2605
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Country [7]
279155
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
288623
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Hunter New England Health Research Ethics Committee
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Ethics committee address [1]
288623
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Locked Bag 1 New Lambton NSW 2305
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Ethics committee country [1]
288623
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Australia
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Date submitted for ethics approval [1]
288623
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Approval date [1]
288623
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24/10/2012
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Ethics approval number [1]
288623
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12/10/17/3.04
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Ethics committee name [2]
295676
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ACT Health Human Research Ethics Committee
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Ethics committee address [2]
295676
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Building 10, Level 6 Canberra Hospital PO Box 11, Woden ACT 2606
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Ethics committee country [2]
295676
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Australia
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Date submitted for ethics approval [2]
295676
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Approval date [2]
295676
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10/12/2015
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Ethics approval number [2]
295676
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ETH.11.15.232
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Summary
Brief summary
This study in pregnant women with asthma investigates the maternal, infant and childhood outcomes following asthma treatment adjustment using FENO, compared to standardised usual care treatment adjustment.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
34832
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Prof Peter Gibson
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Address
34832
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Centre for Asthma and Respiratory Diseases
Level 2, West Wing
Hunter Medical Research Institute
Locked Bag 1,
HRMC
Newcastle NSW 2310
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Country
34832
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Australia
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Phone
34832
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61 02 40420143
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Fax
34832
0
61 02 40420046
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Email
34832
0
[email protected]
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Contact person for public queries
Name
18079
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Prof Peter Gibson
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Address
18079
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Centre for Asthma and Respiratory Diseases
Level 2, West Wing
Hunter Medical Research Institute
Locked Bag 1,
HRMC
Newcastle NSW 2310
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Country
18079
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Australia
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Phone
18079
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61 02 40420143
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Fax
18079
0
61 02 40420046
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Email
18079
0
[email protected]
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Contact person for scientific queries
Name
9007
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Prof Peter Gibson
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Address
9007
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Centre for Asthma and Respiratory Diseases
Level 2, West Wing
Hunter Medical Research Institute
Locked Bag 1,
HRMC
Newcastle NSW 2310
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Country
9007
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Australia
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Phone
9007
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61 02 40420143
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Fax
9007
0
61 02 40420046
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Email
9007
0
[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
We have selected no at this time, but may change to yes in the future
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
4239
Ethical approval
[email protected]
4507
Study protocol
[email protected]
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Interventions for managing asthma in pregnancy.
2014
https://dx.doi.org/10.1002/14651858.CD010660.pub2
Embase
Observational study of mental health in asthmatic women during the prenatal and postnatal periods.
2020
https://dx.doi.org/10.1080/02770903.2019.1621888
Embase
Effect of asthma management with exhaled nitric oxide versus usual care on perinatal outcomes.
2022
https://dx.doi.org/10.1183/13993003.00298-2022
Embase
Higher exhaled nitric oxide at 6 weeks of age is associated with less bronchiolitis and wheeze in the first 12 months of age.
2022
https://dx.doi.org/10.1136/thoraxjnl-2021-217299
N.B. These documents automatically identified may not have been verified by the study sponsor.
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