Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12619000904178
Ethics application status
Approved
Date submitted
12/03/2019
Date registered
27/06/2019
Date last updated
2/03/2023
Date data sharing statement initially provided
27/06/2019
Date results provided
1/06/2022
Type of registration
Prospectively registered

Titles & IDs
Public title
Validity of pulsatile flow assessment by carotid artery ultrasound
Scientific title
Assessing the validity of two-dimensional ultrasound to detect the presence or absence of a pulse
Secondary ID [1] 297706 0
None
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
cardiac arrest 312010 0
Condition category
Condition code
Emergency medicine 310577 310577 0 0
Resuscitation

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Ten-second two-dimension ultrasound videos of the carotid artery at mean arterial pressure of 20-30mmHg, 40-50mmHg, 60-70 mmHg during cardiac surgery off bypass to be reviewed by critical care resident doctor
Intervention code [1] 313937 0
Diagnosis / Prognosis
Comparator / control treatment
The gold standard / comparator will be the presence of a pulse on an arterial line. When we collect the ultrasound images we will know if a pulse is present or not and this will be used to determine whether an video has a pulse or not, against which the physician-readers will be compared
Control group
Active

Outcomes
Primary outcome [1] 319430 0
Specificity of carotid ultrasound to detect no pulse as assessed by detection of no pulse in patients not on bypass when compared to there also being no pulse on the arterial line, for the total sample
Timepoint [1] 319430 0
in ten seconds
Primary outcome [2] 319757 0
Sensitivity of carotid ultrasound to detect a pulse as assessed by detection of a pulse in patients not on bypass when compared to there also being a pulse on the arterial line for the total sample
Timepoint [2] 319757 0
at 10 seconds
Secondary outcome [1] 368149 0
a comparison of the specificity of carotid ultrasound to detect no pulse as assessed by detection of no pulse in patients not on bypass for each mean arterial pressure range (20-30mmHg, 40-50mmHg, 60-70 mmHg) compared to the presence / absence of a pulse on the arterial line, as assessed by Youdin's Index
Timepoint [1] 368149 0
10 seconds
Secondary outcome [2] 368151 0
a comparison of the sensitivity of carotid ultrasound to detect no pulse as assessed by detection of no pulse in patients not on bypass for each mean arterial pressure range (20-30mmHg, 40-50mmHg, 60-70 mmHg) compared to the presence / absence of a pulse on the arterial line, as assessed by Youdin's Index
Timepoint [2] 368151 0
10 seconds

Eligibility
Key inclusion criteria
There will be two groups of participants:

1. Carotid ultrasound participants. These participants will be from consenting cardiac surgery volunteers. All cardiac surgery patients who will be placed on bypass during their surgery, including valve replacement or coronary artery bypass grafts. Age > 18. Ability to offer informed consent.

2. Critical care physician readers. These participants will be consenting volunteer critical care physicians who will be asked to review a maximum of 30 of the carotid ultrasound video clips. Any post-graduate critical care physician who uses ultrasound in their clinical practice, whether for focussed echocardiography, central line placement or trauma assessment.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Cardiac surgery participants: Previous surgery involving the great blood vessels including aorta or carotid arteries. Patients who the cardiac surgeon considers to be inappropriate due to a high surgical risk, patients with an intra-aortic balloon pump, and patients with known carotid artery stenosis.

Critical care physician readers: No previous experience with ultrasound.

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
The randomisation will be the order in which the ultrasound scans are presented to the readers. Readers of the ultrasound scans will not know whether the images they are viewing have a pulse or not, nor the ratio of pulse to no-pulse in the images they review. The entire sample of ultrasound images will be block randomised, so that the order is different for each reader, but each scan is not reviewed more than once by an individual reader.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
will be by R code : RandomSeq <- as.data.frame(block.random(n=x, c(video =y, iter =z)))
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?


The people assessing the outcomes
Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
All data analysis will be performed using R statistical analysis software. Diagnostic test criteria will be generated an analysed using the epitests package. Youden’s index and the comparison of Youden’s index between different mean arterial pressure will be performed using either the cutpoint R or optimalcutpoints packages and also the DTCompare package. A significance level of 0.05 will be considered significant.

Missing data plan.

We plan to reduce the amount of potential missing data by collecting only information relevant to the study and its outcomes.

As this is a paired-patient study, ideally we will collect a video from all three MAP ranges (20-30mmHg, 40-50mmHg, 60-70 mmHg) from each patient. In the situation where we are not able to collect all three MAP ranges from each patient, we will use a complete case analysis approach and removing all of the patient in who three videos could not be obtained. It is anticipated that this will occur infrequently, so that in seeking a maximum of 30 patients we should obtain all four videos for our minimum sample size of 24.

If we cannot obtain a carotid US video of the three MAP ranges in more than six patients, we will then look at either widening the MAP ranges in subsequent videos or changing to an available-case approach and combining all available videos so that the final video data-set has an equal proportion of videos numbers per MAP range, but in an unpaired approach. This would not alter the method of analysis but would reduce the power of the study. Of this were to occur we would consult a statistician for advice on the number of readers than would be required to adequately power the study (something we could not do until after the carotid US videos are collected).

Recruitment
Recruitment status
Stopped early
Data analysis
Data analysis is complete
Reason for early stopping/withdrawal
Other reasons/comments
Other reasons
COVID-19 prevented us form reaching full sample size for carotid US patients
Date of first participant enrolment
Anticipated
30/09/2019
Actual
4/10/2019
Date of last participant enrolment
Anticipated
Actual
13/05/2020
Date of last data collection
Anticipated
Actual
13/05/2020
Sample size
Target
30
Accrual to date
Final
29
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 13371 0
St George Hospital - Kogarah
Recruitment postcode(s) [1] 25971 0
2217 - Kogarah

Funding & Sponsors
Funding source category [1] 302230 0
Hospital
Name [1] 302230 0
St George Hospital, Kogarah
Country [1] 302230 0
Australia
Primary sponsor type
Hospital
Name
St George Hospital, Kogarah
Address
Gray St,
Kogarah
2217 NSW, Australia
Country
Australia
Secondary sponsor category [1] 302085 0
None
Name [1] 302085 0
Address [1] 302085 0
Country [1] 302085 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 302910 0
South Eastern Sydney Local Health District Human Research Ethics Committee
Ethics committee address [1] 302910 0
Ethics committee country [1] 302910 0
Australia
Date submitted for ethics approval [1] 302910 0
01/05/2019
Approval date [1] 302910 0
25/09/2019
Ethics approval number [1] 302910 0
2019/ETH00568

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

Contacts
Principal investigator
Name 91814 0
Dr Matthew Miller
Address 91814 0
Department of Anaesthesia
St George Hospital
Gray St,
Kogarah
NSW 2217
Country 91814 0
Australia
Phone 91814 0
+61 2 9113 1111
Fax 91814 0
Email 91814 0
[email protected]
Contact person for public queries
Name 91815 0
Matthew Miller
Address 91815 0
Department of Anaesthesia
St George Hospital
Gray St,
Kogarah
NSW 2217
Country 91815 0
Australia
Phone 91815 0
+61 2 9113 1111
Fax 91815 0
Email 91815 0
[email protected]
Contact person for scientific queries
Name 91816 0
Matthew Miller
Address 91816 0
Department of Anaesthesia
St George Hospital
Gray St,
Kogarah
NSW 2217
Country 91816 0
Australia
Phone 91816 0
+61 2 9113 1111
Fax 91816 0
Email 91816 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
they will be mostly large video files which will be too big to share, however we will be asking permission to share the data from participants. If the ethics committee agree that we can share the data with the participants permission, we will do so


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
SourceTitleYear of PublicationDOI
EmbaseAssessing the validity of two-dimensional carotid ultrasound to detect the presence and absence of a pulse.2020https://dx.doi.org/10.1016/j.resuscitation.2020.10.002
N.B. These documents automatically identified may not have been verified by the study sponsor.