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Trial registered on ANZCTR
Registration number
ACTRN12606000258550
Ethics application status
Approved
Date submitted
2/05/2001
Date registered
2/05/2001
Date last updated
2/05/2001
Type of registration
Retrospectively registered
Titles & IDs
Public title
Should very premature babies be treated at birth with intubation and ventilation or just a continuous positive pressure into the nose?
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Scientific title
Nasal CPAP (continuous positive airway pressure) for very preterm infants at birth: Does it reduce the incidence of chronic lung disease? A randomised controlled trial.
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Secondary ID [1]
27
0
Perinatal Trials Registry: PTR368
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Universal Trial Number (UTN)
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Trial acronym
COIN148002 (NHMRC application number)
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Very premature infants
27
0
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Chronic lung disease (CLD)
28
0
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Condition category
Condition code
Reproductive Health and Childbirth
31
31
0
0
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Childbirth and postnatal care
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Respiratory
32
32
0
0
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Other respiratory disorders / diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
This project is a definitive randomised controlled trial of early CPAP in preterm infants of 25 to 28 weeks' gestation comparing CPAP at birth with intubation and ventilation at birth.
1. Nasal CPAP (continuous positive pressure) - applying oxygen under a low continuous positive pressure through the nose.
2. Intubation and ventilation - support from an infant ventilator with pressure delivered via a tube in the wind pipe (trachea).
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Intervention code [1]
1098
0
Treatment: Devices
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Comparator / control treatment
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Control group
Active
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Outcomes
Primary outcome [1]
58
0
Death while in neonatal unit. Reduction from 30% to 20%.
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Assessment method [1]
58
0
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Timepoint [1]
58
0
At 36 weeks
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Primary outcome [2]
59
0
Iincidence of chronic lung disease. Reduction from 30% to 20%.
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Assessment method [2]
59
0
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Timepoint [2]
59
0
At 36 weeks
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Secondary outcome [1]
87
0
1. The incidence of intubation and ventilation
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Assessment method [1]
87
0
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Timepoint [1]
87
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Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [2]
88
0
2. Reasons for intubation and ventilation
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Assessment method [2]
88
0
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Timepoint [2]
88
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Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [3]
89
0
3. The incidence of air leaks
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Assessment method [3]
89
0
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Timepoint [3]
89
0
Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [4]
90
0
4. The incidence of intracranial haemorrhages
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Assessment method [4]
90
0
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Timepoint [4]
90
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Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [5]
91
0
5. Time receiving ventilation
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Assessment method [5]
91
0
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Timepoint [5]
91
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Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [6]
92
0
6. Time receiving nasal CPAP
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Assessment method [6]
92
0
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Timepoint [6]
92
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Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [7]
93
0
7. Time in hospital
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Assessment method [7]
93
0
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Timepoint [7]
93
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Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [8]
94
0
8. Time to regain birth weight
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Assessment method [8]
94
0
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Timepoint [8]
94
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Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [9]
95
0
9. Need for oxygen
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Assessment method [9]
95
0
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Timepoint [9]
95
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At 28 days.
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Secondary outcome [10]
96
0
10. The inspired oxygen
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Assessment method [10]
96
0
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Timepoint [10]
96
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At 36 weeks' gestation.
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Secondary outcome [11]
97
0
11. The use of concomitant methylxanthines
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Assessment method [11]
97
0
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Timepoint [11]
97
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Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [12]
98
0
12. The use of postantal steroids
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Assessment method [12]
98
0
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Timepoint [12]
98
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Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [13]
99
0
13. The nuber of doses of surfactant used
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Assessment method [13]
99
0
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Timepoint [13]
99
0
Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [14]
100
0
14. Economic analysis
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Assessment method [14]
100
0
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Timepoint [14]
100
0
Secondary outcomes are measured during the infants stay in the hospital as they occur.
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Secondary outcome [15]
101
0
15. Respiratory morbidity
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Assessment method [15]
101
0
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Timepoint [15]
101
0
In the first year after discharge.
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Eligibility
Key inclusion criteria
Inborn infants 25 week 0 days to 28 weeks 6 days gestation who breathe at birth & parents consent.
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Minimum age
25
Weeks
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Maximum age
28
Weeks
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Babies who have a condition which might compromise respiration. Don't breathe at birth.
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Study design
Purpose of the study
Treatment
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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)
Sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Treatment allocation will be either to nasal CPAP at 8 cm H2O or to intubation and IPPV. Allocation will be assigned randomly using a random number generator and permuted blocks for each centre. This will be produced by the statistical department of the Royal Children's Hospital. Randomisation will be stratified into two gestational age groups: 25 and 26 weeks', and 27 and 28 weeks'. This will reduce any imbalance in gestational age between the groups and allow analysis of the groups seperately. The assinged treatment will be enclosed in sequentially numbered opaque envelopes. There will be a separate set of envelopes for each gestational age stratum in each centre.
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Factorial
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Other design features
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Phase
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
1/02/2001
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
600
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
42
0
Government body
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Name [1]
42
0
National Health & Medical Research Council
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Address [1]
42
0
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Country [1]
42
0
Australia
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Primary sponsor type
Charities/Societies/Foundations
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Name
Women's and Children's Research Foundation
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Address
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Country
Australia
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Secondary sponsor category [1]
36
0
None
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Name [1]
36
0
Nil
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Address [1]
36
0
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Country [1]
36
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
314
0
The Royal Women's Hospital Research and Ethics Committee
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Ethics committee address [1]
314
0
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Ethics committee country [1]
314
0
Australia
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Date submitted for ethics approval [1]
314
0
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Approval date [1]
314
0
18/03/1999
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Ethics approval number [1]
314
0
98/41
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Ethics committee name [2]
315
0
Royal North Shore hospital NSH Human Research Ethics Committee
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Ethics committee address [2]
315
0
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Ethics committee country [2]
315
0
Australia
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Date submitted for ethics approval [2]
315
0
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Approval date [2]
315
0
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Ethics approval number [2]
315
0
0104-051M
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Ethics committee name [3]
316
0
Royal Women's Hospital Research Ethics Committee
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Ethics committee address [3]
316
0
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Ethics committee country [3]
316
0
Australia
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Date submitted for ethics approval [3]
316
0
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Approval date [3]
316
0
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Ethics approval number [3]
316
0
RWH 01/2
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Ethics committee name [4]
317
0
Montefiore Medical Centre
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Ethics committee address [4]
317
0
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Ethics committee country [4]
317
0
Australia
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Date submitted for ethics approval [4]
317
0
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Approval date [4]
317
0
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Ethics approval number [4]
317
0
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Ethics committee name [5]
318
0
King Edward Memorial and Princess Margaret Hospital
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Ethics committee address [5]
318
0
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Ethics committee country [5]
318
0
Australia
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Date submitted for ethics approval [5]
318
0
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Approval date [5]
318
0
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Ethics approval number [5]
318
0
694/EW
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Ethics committee name [6]
319
0
Alexandra Hospital
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Ethics committee address [6]
319
0
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Ethics committee country [6]
319
0
Australia
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Date submitted for ethics approval [6]
319
0
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Approval date [6]
319
0
01/03/2002
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Ethics approval number [6]
319
0
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Ethics committee name [7]
320
0
Albert Einstein College of Medicine
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Ethics committee address [7]
320
0
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Ethics committee country [7]
320
0
United States of America
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Date submitted for ethics approval [7]
320
0
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Approval date [7]
320
0
20/05/2002
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Ethics approval number [7]
320
0
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Ethics committee name [8]
321
0
Hackensack University Medical Centre
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Ethics committee address [8]
321
0
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Ethics committee country [8]
321
0
United States of America
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Date submitted for ethics approval [8]
321
0
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Approval date [8]
321
0
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Ethics approval number [8]
321
0
02.02.102
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Ethics committee name [9]
322
0
NICU Gent University Hosptial
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Ethics committee address [9]
322
0
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Ethics committee country [9]
322
0
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Date submitted for ethics approval [9]
322
0
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Approval date [9]
322
0
21/01/2003
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Ethics approval number [9]
322
0
2002/350
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Ethics committee name [10]
323
0
Maternite Regionale Universitaire
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Ethics committee address [10]
323
0
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Ethics committee country [10]
323
0
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Date submitted for ethics approval [10]
323
0
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Approval date [10]
323
0
17/04/2003
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Ethics approval number [10]
323
0
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Ethics committee name [11]
324
0
Rikshospitalet University Hospital
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Ethics committee address [11]
324
0
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Ethics committee country [11]
324
0
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Date submitted for ethics approval [11]
324
0
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Approval date [11]
324
0
13/01/2003
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Ethics approval number [11]
324
0
S-02275
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Ethics committee name [12]
325
0
Univ.-Klinikum Freiburg
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Ethics committee address [12]
325
0
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Ethics committee country [12]
325
0
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Date submitted for ethics approval [12]
325
0
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Approval date [12]
325
0
04/12/2003
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Ethics approval number [12]
325
0
Nr 278/03
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Ethics committee name [13]
326
0
Klinik for Neonatologie Charite Mitte
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Ethics committee address [13]
326
0
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Ethics committee country [13]
326
0
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Date submitted for ethics approval [13]
326
0
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Approval date [13]
326
0
06/06/2003
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Ethics approval number [13]
326
0
1943/ /Si272
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Summary
Brief summary
The standard treatment of very premature babies has been intubation and ventilation at birth. Recent non-randomised studies have shown that some of these babies can be managed with oxygen provided under a low continuous positive pressure into the nose and that this may improve some of their outcomes. This trial will be the first randomised trial to compare these two treatments and determine which has the optimal outcome for the baby.
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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
35682
0
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Address
35682
0
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Country
35682
0
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Phone
35682
0
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Fax
35682
0
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Email
35682
0
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Contact person for public queries
Name
10287
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Linh Ung
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Address
10287
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The Royal Women's Hospital
University Department of Obstetrics and Gynaecology
132 Grattan Street
Carlton VIC 3053.
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Country
10287
0
Australia
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Phone
10287
0
03 9344 2609
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Fax
10287
0
03 9347 1761
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Email
10287
0
[email protected]
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Contact person for scientific queries
Name
1215
0
Professor Colin Morley
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Address
1215
0
The Royal Women's Hospital
Neonatal Unit 9th Floor
132 Grattan Street
Carlton VIC 3053
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Country
1215
0
Australia
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Phone
1215
0
03 9344 2527
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Fax
1215
0
03 9347 2731
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Email
1215
0
[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
No additional documents have been identified.
Download to PDF