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Trial registered on ANZCTR
Registration number
ACTRN12622000879763p
Ethics application status
Submitted, not yet approved
Date submitted
15/05/2022
Date registered
21/06/2022
Date last updated
21/06/2022
Date data sharing statement initially provided
21/06/2022
Type of registration
Prospectively registered
Titles & IDs
Public title
comparing the effect of a Dextrose solution on the length of labour in women undergoing an induction of labour
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Scientific title
Evaluation of the effect of a Dextrose solution on the length of labour in nulliparous women undergoing an induction of labour - A Randomised controlled trial
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Secondary ID [1]
307133
0
Nil known
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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:
women having induction of labour (IOL)
326309
0
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Prolonged labour
326310
0
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Condition category
Condition code
Reproductive Health and Childbirth
323621
323621
0
0
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Other reproductive health and childbirth disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The intervention group will receive intravenous infusion of 3.3% glucose in 0.3% sodium chloride (33g/l glucose) from time of rupture of membranes in birth suite until delivery of the placenta.
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Intervention code [1]
323589
0
Treatment: Other
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Comparator / control treatment
intravenous infusion of compound sodium lactate (Hartmann’s solution) from the time of rupture of membranes in birth suite until delivery of the placenta at 250 mls per hour.
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Control group
Active
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Outcomes
Primary outcome [1]
331380
0
duration of labour determined by review of the participant's medical record
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Assessment method [1]
331380
0
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Timepoint [1]
331380
0
birth
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Secondary outcome [1]
409665
0
caesarean section rate determined by review of participant's medical records
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Assessment method [1]
409665
0
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Timepoint [1]
409665
0
birth
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Secondary outcome [2]
409666
0
neonatal hypoglycaemia determined by blood tests
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Assessment method [2]
409666
0
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Timepoint [2]
409666
0
at any time during the first 24 hours after birth, assessed 2 hourly for the first 24 hours
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Secondary outcome [3]
409667
0
maternal sodium levels determined by blood tests
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Assessment method [3]
409667
0
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Timepoint [3]
409667
0
4 and 24 hours after birth
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Secondary outcome [4]
410198
0
5 min Apgar score determined by review of particpant's medical records
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Assessment method [4]
410198
0
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Timepoint [4]
410198
0
at 5 minutes after birth
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Secondary outcome [5]
410199
0
admission to special care nursery determined by review of participant's medical records
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Assessment method [5]
410199
0
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Timepoint [5]
410199
0
after birth
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Eligibility
Key inclusion criteria
Nulliparous women
booking BMI 25-40 kg/m2
induction of labour for postdates.
presentation is cephalic
singleton pregnancy.
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Minimum age
16
Years
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
any medical or obstetrical problems
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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)
sequentially numbered sealed opaque envelopes kept locked in birth suite
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computer generated list of random numbers - assignment o intervention or control in groups of 20
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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
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
Chi squared
RR and 95% Confidence intervals
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/07/2022
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Actual
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Date of last participant enrolment
Anticipated
30/06/2023
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Actual
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Date of last data collection
Anticipated
30/08/2023
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Actual
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Sample size
Target
264
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment hospital [1]
22368
0
Ipswich Hospital - Ipswich
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Recruitment postcode(s) [1]
37531
0
4305 - Ipswich
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Funding & Sponsors
Funding source category [1]
311437
0
Hospital
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Name [1]
311437
0
west Moreton health service
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Address [1]
311437
0
1 Chelmsford Avenue, Ipswich, Qld, Australia 4305
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Country [1]
311437
0
Australia
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Primary sponsor type
Hospital
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Name
West Moreton Hospital and Health Service
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Address
1 chelmsford Ave
Ipswich
Queensland 4305
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Country
Australia
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Secondary sponsor category [1]
312832
0
None
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Name [1]
312832
0
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Address [1]
312832
0
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Country [1]
312832
0
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Ethics approval
Ethics application status
Submitted, not yet approved
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Ethics committee name [1]
310915
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West Moreton Hospital and Health Service HREC
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Ethics committee address [1]
310915
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1 chelmsford Ave Ipswich Queensland 4305
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Ethics committee country [1]
310915
0
Australia
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Date submitted for ethics approval [1]
310915
0
21/06/2022
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Approval date [1]
310915
0
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Ethics approval number [1]
310915
0
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Summary
Brief summary
Women normally receive Hartmann's solution in labour we wish to provide them with more energy using a dextrose solution given slowly in labour to see if we can shorten their length of labour and possibly reduce caesarean section rate
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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
119330
0
A/Prof Kassam Mahomed
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Address
119330
0
women's and children's services
Ipswich Hospital
1 Chelmsford Avenue
Ipswich
Queensland 4305
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Country
119330
0
Australia
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Phone
119330
0
+61407034283
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Fax
119330
0
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Email
119330
0
[email protected]
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Contact person for public queries
Name
119331
0
Kassam Mahomed
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Address
119331
0
women's and children's services
Ipswich Hospital
1 Chelmsford Avenue
Ipswich
Queensland 4305
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Country
119331
0
Australia
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Phone
119331
0
+61407034283
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Fax
119331
0
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Email
119331
0
[email protected]
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Contact person for scientific queries
Name
119332
0
Kassam Mahomed
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Address
119332
0
women's and children's services
Ipswich Hospital
1 Chelmsford Avenue
Ipswich
Queensland 4305
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Country
119332
0
Australia
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Phone
119332
0
+61407034283
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Fax
119332
0
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Email
119332
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?
all outcome deidentified data on request
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When will data be available (start and end dates)?
1/9/23 to 30/8/28
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Available to whom?
any research upon request
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Available for what types of analyses?
outcome data for the purpose of any IPD meta analysis
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How or where can data be obtained?
by contacting PI via e mail:
[email protected]
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
16074
Study protocol
from PI - e mail
[email protected]
...
[
More Details
]
384068-(Uploaded-15-05-2022-09-56-32)-Study-related document.docx
16075
Informed consent form
384068-(Uploaded-15-05-2022-09-55-45)-Study-related document.doc
16076
Ethical approval
awaiting submission and approval
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