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Trial registered on ANZCTR


Registration number
ACTRN12614001089628
Ethics application status
Approved
Date submitted
30/09/2014
Date registered
13/10/2014
Date last updated
16/06/2017
Type of registration
Prospectively registered

Titles & IDs
Public title
Comparison of blood collection tubes for blood glucose testing in the diagnosis of gestational diabetes.
Scientific title
For pregnant women, does blood collection into a citrate test tube, when compared to the standard collection procedure of using a fluoride test tube, produce more accurate venous plasma glucose results.
Secondary ID [1] 285423 0
Nil known
Universal Trial Number (UTN)
U1111-1162-3227
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
gestational diabetes 293177 0
Condition category
Condition code
Reproductive Health and Childbirth 293453 293453 0 0
Fetal medicine and complications of pregnancy
Public Health 293454 293454 0 0
Health service research
Metabolic and Endocrine 293487 293487 0 0
Diabetes

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Interventional study comparing 'new' citrate tubes with conventional fluoride tubes for measuring venous plasma glucose levels during the oral glucose tolerance test in pregnancy. Pregnant women will have blood drawn into three test tubes at each time-point (0-hour, 1-hour, and 2-hour) of their routine oral glucose tolerance test taken between 24-28 weeks' gestation. The usual fluoride tube, the 'new' citrate tube, and a gel tube for the reference glucose.
Intervention code [1] 290342 0
Diagnosis / Prognosis
Intervention code [2] 290426 0
Early detection / Screening
Comparator / control treatment
Pregnant women will have blood drawn into three test tubes at each time-point of their routine oral glucose tolerance test. The three tubes will include the usual fluoride tube, the 'new' citrate tube, and a gel tube for the reference glucose. Each woman will be her own control.
Control group
Active

Outcomes
Primary outcome [1] 293272 0
The difference in venous plasma glucose levels measured in mmol/L between the three types of test tube at each time-point (0-hour, 1-hour, and 2-hours) of the oral glucose tolerance test.
Timepoint [1] 293272 0
At the time of enrolment between 24-28 weeks' gestation, at each time-point (0-hour, 1-hour, and 2-hours) of the oral glucose tolerance test.
Secondary outcome [1] 310699 0
% difference in venous plasma glucose levels measured in the three types of test tube at each time point (0-hour, 1-hour, and 2-hours) of the oral glucose tolerance test.
Timepoint [1] 310699 0
At the time of enrolment between 24-28 weeks' gestation, at each time-point (0-hour, 1-hour, and 2-hours) of the oral glucose tolerance test.

Eligibility
Key inclusion criteria
Pregnant women attending for a routine oral glucose tolerance test to screen for gestational diabetes.
Minimum age
No limit
Maximum age
No limit
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
nil

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Other design features
Phase
Not Applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
3/11/2014
Actual
15/12/2014
Date of last participant enrolment
Anticipated
Actual
31/05/2015
Date of last data collection
Anticipated
Actual
31/05/2015
Sample size
Target
15
Accrual to date
Final
16
Recruitment outside Australia
Country [1] 6384 0
New Zealand
State/province [1] 6384 0

Funding & Sponsors
Funding source category [1] 290027 0
University
Name [1] 290027 0
University of Otago Summer Studentship
Country [1] 290027 0
New Zealand
Primary sponsor type
Individual
Name
Ruth Hughes
Address
Department of Obstetrics and Gynaecology,
Christchurch Women's Hospital
Private Bag 4711
Christchurch 8140
Country
New Zealand
Secondary sponsor category [1] 288719 0
Individual
Name [1] 288719 0
Dr Helen Lunt
Address [1] 288719 0
Department of Medicine,
Christchurch Hospital
Private Bag 4710
Christchurch 8140
Country [1] 288719 0
New Zealand

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 291735 0
New Zealand Southern health and disability ethics committee
Ethics committee address [1] 291735 0
Ethics committee country [1] 291735 0
New Zealand
Date submitted for ethics approval [1] 291735 0
02/10/2014
Approval date [1] 291735 0
16/10/2014
Ethics approval number [1] 291735 0
14/NTA/167

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 51798 0
Dr Helen Lunt
Address 51798 0
Department of medicine,
Christchurch Hospital,
Private bag 4710,
Christchurch 8140
Country 51798 0
New Zealand
Phone 51798 0
+64 3 3640640
Fax 51798 0
Email 51798 0
[email protected]
Contact person for public queries
Name 51799 0
Helen Lunt
Address 51799 0
Department of medicine,
Christchurch Hospital,
Private bag 4710,
Christchurch 8140
Country 51799 0
New Zealand
Phone 51799 0
+64 3 3640640
Fax 51799 0
Email 51799 0
[email protected]
Contact person for scientific queries
Name 51800 0
Helen Lunt
Address 51800 0
Department of medicine,
Christchurch Hospital,
Private bag 4710,
Christchurch 8140
Country 51800 0
New Zealand
Phone 51800 0
+64 3 3640640
Fax 51800 0
Email 51800 0
[email protected]

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.