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Trial registered on ANZCTR
Registration number
ACTRN12619000758101
Ethics application status
Approved
Date submitted
4/05/2019
Date registered
22/05/2019
Date last updated
22/05/2019
Date data sharing statement initially provided
22/05/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Spinal cord Position in Neonates At Lumbar puncture (SPINAL)
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Scientific title
Interobserver variability of clinician performed ultrasound to assess the spinal cord termination in neonates
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Secondary ID [1]
296666
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None
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Universal Trial Number (UTN)
U1111-1232-8017
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Trial acronym
SPINE
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Termination of spinal cord
312700
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Condition category
Condition code
Neurological
311201
311201
0
0
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Other neurological disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The participants will be infants admitted to the hospital who require lumbar puncture. There are no exclusions.
The spinal cord will be examined by ultrasound using linear array probe in mid sagittal (up and down the body) and transverse planes (across the body) and location of the termination of the spinal cord defined in relation to surrounding vertebral bodies.
Ultrasound examinations will be performed by 2 practitioners, Neonatal Consultants or Senior Neonatal Trainees who are experienced in the use of ultrasound. They will have training in the method for examination of the spine and will be allowed to familiarise themselves with this technique.
The procedure will be performed twice by the first observer and twice by a second observer who is blinded to the results of the first. Each observation should take approximately 5 minutes to complete and will occur on the same day.
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Intervention code [1]
314374
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Treatment: Devices
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Intervention code [2]
314523
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Early detection / Screening
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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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Interobserver variability of clinician performed ultrasound to determine the end of the spinal cord.
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Assessment method [1]
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Timepoint [1]
319961
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Study completion
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Secondary outcome [1]
369992
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Infant tolerance of procedure (number of events of cardioresp instability documented on continuous monitoring)
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Assessment method [1]
369992
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Timepoint [1]
369992
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At the time of ultrasound
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Secondary outcome [2]
370404
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perception of infant comfort qualitatively rated by primary nurse/midwife using a scale rating infant comfort 1-3 (1=uncomfortable, 2=neutral, 3=comfortable)
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Assessment method [2]
370404
0
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Timepoint [2]
370404
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at the time of ultrasound
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Eligibility
Key inclusion criteria
The participants will be infants admitted to the hospital who require lumbar puncture.
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Minimum age
0
Days
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Maximum age
6
Months
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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
There are no exclusions.
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Study design
Purpose of the study
Educational / counselling / training
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
NA
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
NA
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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
Single group
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
Primary outcome: Interobserver variability of clinician performed ultrasound to determine the end of the spinal cord.
This will be reported as a mean, standard deviation of the difference.
For the continuous variables of spinal cord level, intraclass correlation (ICC) will be calculated as a measure of reliability. ICC is interpreted as <0.40=poor, 0.40 to 0.75=fair to good and >0.75=excellent reliability. Bland-Altman plots with 95% limits of agreement (LOA) are calculated as a measure of absolute agreement.
Secondary outcomes: Infant tolerance of procedure) and perception of infant comfort rated by primary nurse/midwife.
This will be reported qualitatively.
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/08/2019
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Actual
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Date of last participant enrolment
Anticipated
1/01/2020
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Actual
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Date of last data collection
Anticipated
1/01/2020
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
SA
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Recruitment hospital [1]
13686
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Womens and Childrens Hospital - North Adelaide
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Recruitment postcode(s) [1]
26376
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5006 - North Adelaide
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
301245
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Women's and Children's Hospital
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Address [1]
301245
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72 King William Street
North Adelaide SA 5006
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Country [1]
301245
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Australia
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Primary sponsor type
Individual
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Name
Lydia Kennedy
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Address
Women's and Children's Hospital
Department of Neonatal Medicine
72 King William Street
North Adelaide SA 5006
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Country
Australia
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Secondary sponsor category [1]
300880
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Hospital
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Name [1]
300880
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Women's and Children's Hospital
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Address [1]
300880
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72 King William Street
North Adelaide SA 5006
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Country [1]
300880
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Women's and Children's Health Network Human Research Ethics Committee
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Ethics committee address [1]
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Research Secreteriate Level 2 Samuel Way Building 72 King William Road North Adelaide SA 5006
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Ethics committee country [1]
301984
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Australia
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Date submitted for ethics approval [1]
301984
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20/11/2018
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Approval date [1]
301984
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05/02/2019
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Ethics approval number [1]
301984
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HREC/18/WCHN/163
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Summary
Brief summary
Aim: To determine the interobserver variability of ultrasound of the spinal cord performed on infants by clinicians. Hypothesis: We hypothesise that clinician performed ultrasound reliably and reproducibly identifies the end of the spinal cord in newborn infants. If reliable, the use of spinal ultrasound would enhance the safety of infants undergoing lumbar puncture by ensuring that the location of puncture occurs below the end of the spinal cord thus eliminating the risk of cord injury.
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Trial website
None
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Trial related presentations / publications
None
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Public notes
None
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Contacts
Principal investigator
Name
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Dr Lydia Kennedy
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Address
88762
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Department of Neonatology
Women's and Children's Hospital
72 King William Street
North Adelaide SA 5006
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Country
88762
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Australia
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Phone
88762
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+61 8 81617000
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Fax
88762
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Email
88762
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[email protected]
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Contact person for public queries
Name
88763
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Lydia Kennedy
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Address
88763
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Department of Neonatology
Women's and Children's Hospital
72 King William Street
North Adelaide SA 5006
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Country
88763
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Australia
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Phone
88763
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+61 8 81617000
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Fax
88763
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Email
88763
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[email protected]
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Contact person for scientific queries
Name
88764
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Lydia Kennedy
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Address
88764
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Department of Neonatology
Women's and Children's Hospital
72 King William Street
North Adelaide SA 5006
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Country
88764
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Australia
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Phone
88764
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+61 8 81617000
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Fax
88764
0
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Email
88764
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
Not approved by ethics committee
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
1993
Ethical approval
376426-(Uploaded-04-05-2019-15-06-48)-Study-related document.pdf
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