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Trial registered on ANZCTR
Registration number
ACTRN12620000449932
Ethics application status
Approved
Date submitted
4/04/2020
Date registered
6/04/2020
Date last updated
6/04/2020
Date data sharing statement initially provided
6/04/2020
Type of registration
Prospectively registered
Titles & IDs
Public title
Maternal and neonatal outcomes from women infected with SARS-COV2 (COVID-19) during pregnancy
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Scientific title
Prospective registry of maternal, perinatal and neonatal outcomes from pregnancies infected with SARS-COV2 (COVID-19)
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Secondary ID [1]
300948
0
None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Pregnancy
316962
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COVID-19 infection
316963
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Condition category
Condition code
Reproductive Health and Childbirth
315117
315117
0
0
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Childbirth and postnatal care
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Reproductive Health and Childbirth
315118
315118
0
0
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Complications of newborn
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Reproductive Health and Childbirth
315119
315119
0
0
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Fetal medicine and complications of pregnancy
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Infection
315120
315120
0
0
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Other infectious diseases
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Respiratory
315134
315134
0
0
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Other respiratory disorders / diseases
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Intervention/exposure
Study type
Observational
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Patient registry
True
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Target follow-up duration
2
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Target follow-up type
Years
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Description of intervention(s) / exposure
All women infected with SARS-CoV 2 (novel coronavirus) infection or who were diagnosed with COVID-19 during pregnancy. Observation will continue throughout pregnancy up until 6 weeks postpartum. In addition to standard care, women will be asked to complete a questionnaire after discharge to include postpartum and neonatal outcomes.
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Intervention code [1]
317266
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Not applicable
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Maternal mortality from COVID-19
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Assessment method [1]
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Timepoint [1]
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During pregnancy until 6 weeks postpartum
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Primary outcome [2]
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Perinatal mortality (stillbirth, neonatal death)
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Assessment method [2]
323397
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Timepoint [2]
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During pregnancy and until day 28 in the neonate
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Secondary outcome [1]
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Composite maternal morbidity from COVID-19 recorded from medical records. Including:
Hospitalisation for complications of COVID-19 (respiratory/pregnancy related)
ICU admission
Respiratory failure - need for NIV invasive ventilation
Renal failure - requiring dialysis
Coagulopathy inc DIC
Sepsis
Postpartum haemorrhage > 500 ml
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Assessment method [1]
381786
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Timepoint [1]
381786
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Pregnancy until 6 weeks postpartum
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Secondary outcome [2]
381787
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Confirmed vertical transmission - SARs-COV2 PCR positive or positive serology result in any of:
Cord blood
Placenta
Amniotic fluid
Neonatal testing
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Assessment method [2]
381787
0
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Timepoint [2]
381787
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Until day 28 of life
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Secondary outcome [3]
381788
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Mode of delivery - data collected as part of routine medical care
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Assessment method [3]
381788
0
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Timepoint [3]
381788
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At birth
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Secondary outcome [4]
381837
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Composite neonatal morbidity:
NICU admission - medical record,
Respiratory distress - requiring > 12 hours NIV or intubation
Sepsis - requiring supportive care and treatment
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Assessment method [4]
381837
0
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Timepoint [4]
381837
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Until day 28 or discharge from hospital
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Secondary outcome [5]
381838
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Congenital anomaly diagnosed in fetus or neonate: on imaging (ultrasound or MRI), genetic testing (karyotype, microarray), at post-mortem or by physical examination.
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Assessment method [5]
381838
0
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Timepoint [5]
381838
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Diagnosed during pregnancy or in neonate
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Eligibility
Key inclusion criteria
All pregnant women admitted to a participating hospital with COVID-19 during pregnancy
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Minimum age
18
Years
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Maximum age
60
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Suspected COVID-19 not subsequently confirmed on PCR, serology or imaging
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Descriptive statistics will be reported using frequencies and percentages or proportions for binary or categorical data. Percentages will be calculated based upon the number of patients for whom data are available. Continuous or dimensional variables will be summarised using means and standard deviations, with medians and interquartile ranges ( reported for potentially skewed data. Monthly incidence data and pregnancy outcome data will be calculated and reported to participating sites and national governance.
All analyses will be conducted using standard professional statistical software, such as Stata (Stata Corporation, College Station, Texas).
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
10/04/2020
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Actual
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Date of last participant enrolment
Anticipated
1/04/2021
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Actual
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Date of last data collection
Anticipated
31/12/2021
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Actual
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Sample size
Target
200
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,NT,QLD,SA,TAS,WA,VIC
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Recruitment hospital [1]
16373
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The Royal Women's Hospital - Parkville
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Recruitment hospital [2]
16374
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Monash Medical Centre - Clayton campus - Clayton
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Recruitment hospital [3]
16375
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Mercy Hospital for Women - Heidelberg
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Recruitment hospital [4]
16377
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Royal Hobart Hospital - Hobart
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Recruitment hospital [5]
16378
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Flinders Medical Centre - Bedford Park
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Recruitment hospital [6]
16379
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Womens and Childrens Hospital - North Adelaide
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Recruitment hospital [7]
16380
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King Edward Memorial Hospital - Subiaco
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Recruitment hospital [8]
16381
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Westmead Hospital - Westmead
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Recruitment hospital [9]
16382
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Royal Hospital for Women - Randwick
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Recruitment hospital [10]
16383
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Royal Prince Alfred Hospital - Camperdown
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Recruitment hospital [11]
16384
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John Hunter Hospital - New Lambton
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Recruitment hospital [12]
16385
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Royal Darwin Hospital - Tiwi
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Recruitment hospital [13]
16386
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Mater Sydney - North Sydney
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Recruitment hospital [14]
16387
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Sunshine Coast University Hospital - Birtinya
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Recruitment hospital [15]
16388
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Royal Brisbane & Womens Hospital - Herston
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Recruitment postcode(s) [1]
29917
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3052 - Parkville
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Recruitment postcode(s) [2]
29918
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3168 - Clayton
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Recruitment postcode(s) [3]
29919
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3084 - Heidelberg
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Recruitment postcode(s) [4]
29921
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7000 - Hobart
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Recruitment postcode(s) [5]
29922
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5042 - Bedford Park
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Recruitment postcode(s) [6]
29923
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5006 - North Adelaide
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Recruitment postcode(s) [7]
29924
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6008 - Subiaco
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Recruitment postcode(s) [8]
29925
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2145 - Westmead
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Recruitment postcode(s) [9]
29926
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2031 - Randwick
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Recruitment postcode(s) [10]
29927
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2050 - Camperdown
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Recruitment postcode(s) [11]
29928
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2305 - New Lambton
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Recruitment postcode(s) [12]
29929
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0810 - Tiwi
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Recruitment postcode(s) [13]
29930
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2060 - North Sydney
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Recruitment postcode(s) [14]
29931
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4575 - Birtinya
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Recruitment postcode(s) [15]
29932
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4029 - Herston
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Funding & Sponsors
Funding source category [1]
305389
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University
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Name [1]
305389
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University of Melbourne
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Address [1]
305389
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Royal Women's Hospital
Flemington Road
Parkville
VIC 3052
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Country [1]
305389
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Australia
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Primary sponsor type
University
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Name
University of Melbourne
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Address
Pregnancy Research Centre
Royal Women's Hospital
Flemington Road
Parkville
VIC 3052
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Country
Australia
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Secondary sponsor category [1]
305771
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University
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Name [1]
305771
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Monash University
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Address [1]
305771
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Department of Obstetrics and Gynaecology
Monash Medical Centre
Clayton Road
Clayton
VIC 3168
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Country [1]
305771
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
305720
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Monash Health Human Research Ethics Committee A
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Ethics committee address [1]
305720
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Monash Health 246 Clayton Road Clayton VIC 3168
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Ethics committee country [1]
305720
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Australia
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Date submitted for ethics approval [1]
305720
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27/03/2020
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Approval date [1]
305720
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02/04/2020
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Ethics approval number [1]
305720
0
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Summary
Brief summary
This is a national study of women with confirmed COVID-19 in pregnancy in Australia. The study will collect information about all pregnant women who are confirmed to have SARS- CoV2 infection. The information will be analysed on a continuous basis to inform ongoing guidance for women and maternity staff as we respond to the pandemic. Specifically, the study will describe incidence, management and outcomes of COVID-19 in pregnancy and identify factors associated with better outcomes for women and their babies. Anonymous information will be collected by clinicians or clinical researchers who are based in maternity units in the Australia. Data collectors will have been sent a live link to a RedCap database to allow them to notify cases and complete an anonymous data collection form. SARs-COV-2 is a new strain of coronavirus that has not previously been identified in humans. which causes a respiratory illness, but it is not known what impact it will have on pregnant women and their babies. In order to investigate risk factors, management and outcomes, the researchers plan to extend data collection to include data on all pregnant women with SARS-CoV-2. The aim of this study is to learn more about the effects of SARS-COV-2 and its treatment on pregnant women and their babies. Pregnant women, are known to be at increased risk of developing more serious problems from respiratory viral infections, as was shown in the MERs, SARS and H1N1 'swine flu' epidemics. But little is currently known about this virus. This study will collect and report contemporary data to inform ongoing pregnancy and neonatal management in order to optimise modifiable outcomes.
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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
101346
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Dr Clare Whitehead
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Address
101346
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Pregnancy research centre
University of Melbourne
Royal Women's Hospital
Flemington Road
Parkville
VIC 3052
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Country
101346
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Australia
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Phone
101346
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+61 3 8345 2000
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Fax
101346
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Email
101346
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[email protected]
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Contact person for public queries
Name
101347
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Miranda Davies-Tuck
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Address
101347
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Hudson Institute of Medical Research
27-31 Wright St
Clayton
VIC 3168
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Country
101347
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Australia
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Phone
101347
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+61 3 8572 2700
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Fax
101347
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Email
101347
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[email protected]
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Contact person for scientific queries
Name
101348
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Clare Whitehead
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Address
101348
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Pregnancy research centre
University of Melbourne
Royal Women's Hospital
Flemington Road
Parkville
VIC 3052
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Country
101348
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Australia
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Phone
101348
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+61 3 8345 2000
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Fax
101348
0
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Email
101348
0
[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
De-identified clinical outcome data collected
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When will data be available (start and end dates)?
From commencement of study individual participant data (if pregnancy completed) will be publicly available. No end date determined.
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Available to whom?
Collaborators with HREC approved relevant research proposals
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Available for what types of analyses?
For the aims in approved proposals
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How or where can data be obtained?
Subject to approval by the PIs. Please contact via email:
[email protected]
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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.
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