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Trial registered on ANZCTR
Registration number
ACTRN12616001484437
Ethics application status
Approved
Date submitted
21/10/2016
Date registered
25/10/2016
Date last updated
24/08/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Performance comparison between ECG-gated 7 Tesla and clinical 1.5 Tesla Cardiac Magnetic Resonance Imaging in patients with cardiac scar tissue
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Scientific title
7 Tesla UltraHigh Field ECG-gated Cardiac Magnetic Resonance Imaging in non-stented patients with cardiac scar tissue, for left ventricular (LV) and right ventricular (RV) volumetric assessment and scar quantitation
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Secondary ID [1]
290314
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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:
cardiac scar tissue from a prior myocardial infarct (MI) or a non-ischaemic myocardial injury (such as HCM, myocarditis or sarcoid), in patients without coronary artery stents
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Condition category
Condition code
Cardiovascular
300430
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0
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Other cardiovascular diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
7 Tesla (7T) Ultra-High Field Cardiac Magnetic Resonance Imaging (CMRI)
Participants will be recruited from patients with cardiac scar tissue undergoing routine clinical CMRI with gadolinium contrast agent at 1.5 Tesla. All recruited subjects will have an additional 7T CMRI with gadolinium contrast agent.
CMRI is a painless, non-invasive test that involves lying in a scanner. Each patient will first undergo one 1.5T scan of approximately 1 hour duration as part of their normal clinical care. Within 4 weeks of their clinical scan, consenting participants will be asked to come to the imaging facility at The Centre for Advanced Imaging, The University of Queensland. There they will undergo one additional 7T CMRI scan of approximately 1 hour duration.
The results of the clinical 1.5T CMRI scan and the experimental 7T CMRI scan will be compared to
1. evaluate the performance of 7T CMRI compared with standard CMRI at 1.5 T.
2. determine whether 7T CMRI can provide adequate images to measure heart function and scar tissue imaging.
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Intervention code [1]
296196
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Diagnosis / Prognosis
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Comparator / control treatment
The 7T experimental scan is compared to a 1.5T clinical scan, performed on the same patient. The clinical CMRI scan, used as a comparator, is performed at 1.5 Tesla magnetic field strength with injection of gadolinium contrast agent and has a duration of approximately 1 hour. LV and RV volumes and the presence/absence of myocardial enhancement are assessed.
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Control group
Active
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Outcomes
Primary outcome [1]
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Sensitivity and specificity of 7T in comparison to 1.5T
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Assessment method [1]
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Timepoint [1]
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At time of second scan
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Secondary outcome [1]
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Quantitation of myocardial enhancement (FWHM or signal thresholding) at 1.5T vs 7T
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Assessment method [1]
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Timepoint [1]
328590
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at time of second scan
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Eligibility
Key inclusion criteria
Patients scheduled for a clinical CMRI on 1.5T MR scanner, having scar tissue from a prior myocardial infarct (MI) or a non-ischaemic myocardial injury (such as HCM, myocarditis or sarcoid)
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Minimum age
18
Years
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Maximum age
No limit
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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
(1) Subject has MRI non-conditional metal implant, such as a pacemaker
(2) Subject has significant kidney impairment;
(3) Subject has coronary artery stent implanted;
(4) Subject has severe allergy to Gadolinium (Gd) contrast agent;
(5) Subject has claustrophobia;
(6) Subject is pregnant or breastfeeding;
(7) Subject is less than 18 years old.
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Study design
Purpose of the study
Diagnosis
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
Crossover
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
The following parameters will be measured and calculated from CMRI results:
1. Left ventricular (LV) volume fraction and ejection fraction (LVEF);
2. Right ventricular (RV) volume fraction and ejection fraction (RVEF);
3. Left ventricular mass (LV mass);
4. Pulmonary artery flow and stroke volume;
5. Aortic flow and stroke volume;
6. Non-contrast Native T1 mapping (if available);
7. End-diastolic mass;
8. End-systolic mass and;
9. Extracellular volume fraction.
An ANOVA will be carried out to test whether the measurements of each participant are internally consistent (for example, arterial stroke volumes are similar to ventricular stroke volumes) and across magnetic field strength. The multiple comparisons problem will be controlled using a Bonferroni adjustment, with the Family Wise Error Rate restricted to 0.05.
Finally, the Bland-Altman method will be used to examine the relationship between the measurements of the parameters at different field strength (that is, 1.5T versus 7.0T).
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
9/01/2017
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Actual
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Date of last participant enrolment
Anticipated
28/02/2017
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Actual
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Date of last data collection
Anticipated
31/03/2017
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Actual
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Sample size
Target
10
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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]
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The Prince Charles Hospital - Chermside
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Recruitment postcode(s) [1]
14487
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4032 - Chermside
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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The University of Queensland
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Address [1]
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The University of Queensland
Brisbane St Lucia, QLD 4072
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Country [1]
294698
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Australia
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Funding source category [2]
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Charities/Societies/Foundations
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Name [2]
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The Prince Charles Hospital Foundation
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Address [2]
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Level 1, Administration Building
The Prince Charles Hospital, 627 Rode Road, Chermside QLD 4032
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Country [2]
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Australia
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Primary sponsor type
University
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Name
The University of Queensland
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Address
The University of Queensland
Brisbane St Lucia, QLD 4072
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
293544
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Other collaborator category [1]
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Hospital
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Name [1]
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The Prince Charles Hospital
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Address [1]
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The Prince Charles Hospital
627 Rode Road, Chermside QLD 4032
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Country [1]
279266
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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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The Prince Charles Hospital HREC (EC00168)
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Ethics committee address [1]
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The Prince Charles Hospital 627 Rode Road, Chermside QLD 4032
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Ethics committee country [1]
296130
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Australia
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Date submitted for ethics approval [1]
296130
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13/09/2016
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Approval date [1]
296130
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02/11/2016
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Ethics approval number [1]
296130
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HREC/16/QPCH/140
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Ethics committee name [2]
296131
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The University of Queensland Medical Research Ethics Committee (EC00179)
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Ethics committee address [2]
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The University of Queensland Cumbrae-Stewart Building (#72) Brisbane St Lucia 4072
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Ethics committee country [2]
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Australia
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Date submitted for ethics approval [2]
296131
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15/09/2016
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Approval date [2]
296131
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Ethics approval number [2]
296131
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Summary
Brief summary
The research project proposed is to develop cardiac magnetic resonance imaging (CMRI) techniques currently used at standard magnetic field strengths (1.5 or 3 Tesla) for significantly higher field strengths at 7 Tesla (7T). The aims are as follows: 1. To valuate the performance of 7T CMRI compared with standard clinical CMRI at 1.5T. 2. To determine whether 7T CMRI can provide adequate images to measure heart function and cardiac scar imaging. Methods: Participants will be recruited from patients with cardiac scar tissue undergoing routine clinical CMRI with gadolinium contrast agent at 1.5T. All recruited subjects will have an additional 7T CMRI with gadolinium contrast agent. CMRI is a painless, non-invasive test that involves lying in a scanner for a duration of approximately 1 hr. The results of the clinical 1.5T CMRI scan and the experimental 7T CMRI scan will be compared.
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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
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A/Prof Christian Hamilton-Craig
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Address
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Medical Imaging
The Prince Charles Hospital
627 Rode Road, Chermside QLD 4032
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Country
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Australia
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Phone
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+61 7 31395226
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Sabine Fletcher
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Address
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The University of Queensland
Centre for Advanced Imaging, Building 57
St Lucia QLD 4072
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Country
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Australia
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Phone
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+61 7 3365 4100
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Christian Hamilton-Craig
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Address
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Medical Imaging
The Prince Charles Hospital
627 Rode Road, Chermside QLD 4032
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Country
69640
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Australia
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Phone
69640
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+61 7 31395226
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Fax
69640
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Email
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[email protected]
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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.
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