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Trial registered on ANZCTR
Registration number
ACTRN12606000318583
Ethics application status
Approved
Date submitted
5/03/2001
Date registered
5/03/2001
Date last updated
11/01/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
Neonatal respiratory distress syndrome after repeat exposure to antenatal corticosteroids: a randomised controlled trial
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Scientific title
A multicentred randomised controlled trial of repeat doses of prenatal corticosteroid given to women who remain at risk of preterm delivery for the prevention of neonatal morbidity.
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Secondary ID [1]
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Perinatal Trials Registry: PTR349
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Universal Trial Number (UTN)
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Trial acronym
ACTORDS (Australasian Collaborative Trial of Repeat Doses of Corticosteroids for the Prevention of Neonatal Respiratory Disease)
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Women at risk of preterm birth, at less than 32 weeks gestation, who have already received a course of prenatal corticosteroids.
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Condition category
Condition code
Reproductive Health and Childbirth
26
26
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Fetal medicine and complications of pregnancy
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Reproductive Health and Childbirth
27
27
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Antenatal care
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment group: A weekly intramuscular injection of celestone chronodose (2mls, 11.4 mgs) while at risk of preterm birth and if less than 32 weeks gestational age
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Intervention code [1]
1087
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Treatment: Drugs
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Comparator / control treatment
Control Group: A weekly injection of normal saline (2 mls) while at risk of preterm birth and < 32 week gestational age
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Neonatal lung disease
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Assessment method [1]
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Timepoint [1]
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Diagnosed in neonatal period up to hospital discharge
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Primary outcome [2]
54
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Weight, length and head circumference
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Assessment method [2]
54
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Timepoint [2]
54
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Measured at birth and primary hospital discharge.
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Secondary outcome [1]
77
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Maternal infection
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Assessment method [1]
77
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Timepoint [1]
77
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Measured in the antenatal, intrapartum and postnatal periods.
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Secondary outcome [2]
78
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Maternal quality of life
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Assessment method [2]
78
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Timepoint [2]
78
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Measured at 6 months post-partum
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Secondary outcome [3]
79
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Other neonatal morbidity
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Assessment method [3]
79
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Timepoint [3]
79
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Diagnosed in neonatal period up to hospital discharge.
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Eligibility
Key inclusion criteria
Singleton, twin or triplet pregnancy; <32 weeks gestation; > or = 7 days since first corticosteroid treatment, remaining at risk of preterm delivery; informed written signed consent given.
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Minimum age
16
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
Women with chrioamnionitis requiring urgent delivery; Women in whom L/S ratio or equivalent test is judged mature; Women in 2nd stage labour; Women in whom corticosteroid therapy is considered essential.
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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)
Central randomisation by phone.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomisation schedule computer generated with variable block sizes. Treatment allocation stratified by centre, plurality (singleton, twins, triplets), gestational age <28 weeks and >= 28 weeks
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
Safety/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
1/04/1998
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Actual
12/04/1998
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Date of last participant enrolment
Anticipated
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Actual
20/07/2004
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Date of last data collection
Anticipated
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Actual
31/12/2011
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Sample size
Target
980
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Accrual to date
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Final
982
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,QLD,SA,TAS
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Recruitment outside Australia
Country [1]
8565
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New Zealand
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State/province [1]
8565
0
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Funding & Sponsors
Funding source category [1]
34
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Government body
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Name [1]
34
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National Health & Medical Research Council Project Grant
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Address [1]
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National Health and Medical Research Council
GPO Box 1421
Canberra ACT 260
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Country [1]
34
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Australia
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Primary sponsor type
Individual
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Name
Professor Caroline Crowther
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Address
Women's & Children's Hospital
72 King William Rd
North Adelaide SA 5006
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Nil
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Address [1]
31
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Country [1]
31
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Women's & Children's Hospital, Maternal Perinatal Clinical Trials Unit of The University of Adelaide
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Ethics committee address [1]
286
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Ethics committee country [1]
286
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Australia
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Date submitted for ethics approval [1]
286
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Approval date [1]
286
0
01/06/1997
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Ethics approval number [1]
286
0
REC773/4/20060
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Ethics committee name [2]
287
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Royal North Shore Hospital
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Ethics committee address [2]
287
0
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Ethics committee country [2]
287
0
Australia
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Date submitted for ethics approval [2]
287
0
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Approval date [2]
287
0
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Ethics approval number [2]
287
0
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Ethics committee name [3]
288
0
RPA Women's & Babies
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Ethics committee address [3]
288
0
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Ethics committee country [3]
288
0
Australia
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Date submitted for ethics approval [3]
288
0
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Approval date [3]
288
0
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Ethics approval number [3]
288
0
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Ethics committee name [4]
289
0
Royal Hospital for Women
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Ethics committee address [4]
289
0
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Ethics committee country [4]
289
0
Australia
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Date submitted for ethics approval [4]
289
0
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Approval date [4]
289
0
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Ethics approval number [4]
289
0
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Ethics committee name [5]
290
0
John Hunter Hospital
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Ethics committee address [5]
290
0
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Ethics committee country [5]
290
0
Australia
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Date submitted for ethics approval [5]
290
0
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Approval date [5]
290
0
01/09/1998
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Ethics approval number [5]
290
0
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Ethics committee name [6]
291
0
Royal Women's Hospital
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Ethics committee address [6]
291
0
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Ethics committee country [6]
291
0
Australia
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Date submitted for ethics approval [6]
291
0
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Approval date [6]
291
0
01/09/1998
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Ethics approval number [6]
291
0
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Ethics committee name [7]
292
0
Mercy Hospital for Women
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Ethics committee address [7]
292
0
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Ethics committee country [7]
292
0
Australia
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Date submitted for ethics approval [7]
292
0
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Approval date [7]
292
0
01/02/1998
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Ethics approval number [7]
292
0
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Ethics committee name [8]
293
0
Monash Medical Centre
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Ethics committee address [8]
293
0
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Ethics committee country [8]
293
0
Australia
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Date submitted for ethics approval [8]
293
0
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Approval date [8]
293
0
01/07/1998
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Ethics approval number [8]
293
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98062B
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Ethics committee name [9]
294
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Townsville Hospital
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Ethics committee address [9]
294
0
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Ethics committee country [9]
294
0
Australia
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Date submitted for ethics approval [9]
294
0
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Approval date [9]
294
0
01/04/1998
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Ethics approval number [9]
294
0
3/98
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Ethics committee name [10]
295
0
Royal Women's Hospital
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Ethics committee address [10]
295
0
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Ethics committee country [10]
295
0
Australia
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Date submitted for ethics approval [10]
295
0
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Approval date [10]
295
0
01/09/1998
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Ethics approval number [10]
295
0
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Ethics committee name [11]
296
0
Mater Mother's Hospital
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Ethics committee address [11]
296
0
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Ethics committee country [11]
296
0
Australia
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Date submitted for ethics approval [11]
296
0
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Approval date [11]
296
0
01/07/1998
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Ethics approval number [11]
296
0
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Ethics committee name [12]
297
0
Hervey Bay Hospital
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Ethics committee address [12]
297
0
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Ethics committee country [12]
297
0
Australia
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Date submitted for ethics approval [12]
297
0
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Approval date [12]
297
0
01/09/1999
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Ethics approval number [12]
297
0
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Ethics committee name [13]
298
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Toowoomba Hospital
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Ethics committee address [13]
298
0
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Ethics committee country [13]
298
0
Australia
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Date submitted for ethics approval [13]
298
0
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Approval date [13]
298
0
01/10/2000
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Ethics approval number [13]
298
0
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Ethics committee name [14]
299
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Royal Hobart Hospital
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Ethics committee address [14]
299
0
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Ethics committee country [14]
299
0
Australia
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Date submitted for ethics approval [14]
299
0
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Approval date [14]
299
0
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Ethics approval number [14]
299
0
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Ethics committee name [15]
300
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Canberra Hospital
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Ethics committee address [15]
300
0
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Ethics committee country [15]
300
0
Australia
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Date submitted for ethics approval [15]
300
0
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Approval date [15]
300
0
01/09/1998
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Ethics approval number [15]
300
0
ETH.8/98.222
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Ethics committee name [16]
301
0
National Women's Hospital
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Ethics committee address [16]
301
0
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Ethics committee country [16]
301
0
New Zealand
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Date submitted for ethics approval [16]
301
0
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Approval date [16]
301
0
01/10/1998
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Ethics approval number [16]
301
0
98/09/153
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Ethics committee name [17]
302
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Christchurch Women's Hospital
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Ethics committee address [17]
302
0
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Ethics committee country [17]
302
0
New Zealand
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Date submitted for ethics approval [17]
302
0
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Approval date [17]
302
0
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Ethics approval number [17]
302
0
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Ethics committee name [18]
303
0
Waikato Hospital
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Ethics committee address [18]
303
0
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Ethics committee country [18]
303
0
New Zealand
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Date submitted for ethics approval [18]
303
0
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Approval date [18]
303
0
01/04/1998
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Ethics approval number [18]
303
0
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Ethics committee name [19]
304
0
Dunedin Hospital
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Ethics committee address [19]
304
0
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Ethics committee country [19]
304
0
New Zealand
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Date submitted for ethics approval [19]
304
0
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Approval date [19]
304
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01/11/1998
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Ethics approval number [19]
304
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98/07/051
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Ethics committee name [20]
305
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Middlemore Hospital
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Ethics committee address [20]
305
0
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Ethics committee country [20]
305
0
New Zealand
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Date submitted for ethics approval [20]
305
0
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Approval date [20]
305
0
01/06/2001
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Ethics approval number [20]
305
0
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Ethics committee name [21]
306
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Wellington Women's Hospital
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Ethics committee address [21]
306
0
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Ethics committee country [21]
306
0
New Zealand
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Date submitted for ethics approval [21]
306
0
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Approval date [21]
306
0
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Ethics approval number [21]
306
0
01/07/087
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Ethics committee name [22]
307
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Palmerston North Hospital
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Ethics committee address [22]
307
0
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Ethics committee country [22]
307
0
New Zealand
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Date submitted for ethics approval [22]
307
0
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Approval date [22]
307
0
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Ethics approval number [22]
307
0
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Summary
Brief summary
Preterm infants are at high risk of respiratory distress syndrome (RDS) as a consequence of immature lung development. RDS is the principle cause of early mortality and contributes significantly to the high costs of neonatal care. Prenatal corticosteroids substantially reduce the risk of RDS in babies born within 7 days of maternal treatment. Hence, in clinical practice, there has been a tendency to repeat the dose after 7 days in women who remain at risk of preterm birth. However, no formal policy exists. This trial seeks to evaluate the beneficial and adverse effects of repeat doses of prenatal steroids as they may provide a simple, inexpensive way to improve health outcomes for preterm infants. Multi-centre, placebo controlled, double-blind trial. All participants, caregivers, researchers and data analyst are blinded until all prespecified analyses completed. The corticosteroid and saline placebo syringes were identically labelled and the contents masked.
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Trial website
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Trial related presentations / publications
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Public notes
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Attachments [1]
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/AnzctrAttachments/1336-e20160947.full.pdf
(Publication)
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Attachments [2]
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/AnzctrAttachments/1336-1-s2.0-S0140673606688466-main.pdf
(Publication)
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Attachments [3]
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/AnzctrAttachments/1336-nejmoa071152.pdf
(Publication)
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Contacts
Principal investigator
Name
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Prof Caroline Crowther
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Address
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Women's & Children's Hospital
72 King William Rd
North Adelaide SA 5006
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Country
35436
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Australia
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Phone
35436
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+61 8 8161 7619
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Fax
35436
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Email
35436
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[email protected]
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Contact person for public queries
Name
10276
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Caroline Crowther
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Address
10276
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University Obstetrics & Gynaecology
Women's and Children's Hospital
Queen Victoria Building
Level 1
72 King William Road
North Adelaide SA 5006
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Country
10276
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Australia
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Phone
10276
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+61 8 8161 7619
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Fax
10276
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+61 8 8161 7652
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Email
10276
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[email protected]
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Contact person for scientific queries
Name
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Caroline Crowther
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Address
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University Obstetrics & Gynaecology
Women's and Children's Hospital
Queen Victoria Building
Level 1
72 King William Road
North Adelaide SA 5006
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Country
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Australia
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Phone
1204
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+61 8 8161 7619
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Fax
1204
0
+61 8 8161 7652
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Email
1204
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[email protected]
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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
Source
Title
Year of Publication
DOI
Embase
Mid-childhood bone mass after exposure to repeat doses of antenatal glucocorticoids: A randomized trial.
2017
https://dx.doi.org/10.1542/peds.2016-4250
N.B. These documents automatically identified may not have been verified by the study sponsor.
Download to PDF