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Trial registered on ANZCTR
Registration number
ACTRN12619001482156
Ethics application status
Approved
Date submitted
17/10/2019
Date registered
28/10/2019
Date last updated
28/10/2019
Date data sharing statement initially provided
28/10/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Positron Emission Tomography of Oxidative Stress in Friedreich Ataxia
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Scientific title
Non-invasive, in vivo neuroimaging of oxidative stress in Friedreich ataxia
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Secondary ID [1]
299574
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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:
Friedreich ataxia
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Condition category
Condition code
Neurological
313188
313188
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0
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Neurodegenerative diseases
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Human Genetics and Inherited Disorders
313266
313266
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0
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Other human genetics and inherited disorders
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
- Intravenous bolus injection of 125MBq of 64Cu-ATSM, followed by PET scanning of the brain for up to 90mins.
- Single timepoint
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Intervention code [1]
315830
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Early Detection / Screening
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Comparator / control treatment
This observational study will use a cross-sectional, between-group design. A comparator group of individuals who are not affected by Friedreich ataxia, and matched for demographic characteristics, will undergo the same procedures, allowing for between-group statistical comparison with the clinical cohort.
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Control group
Active
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Outcomes
Primary outcome [1]
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Standardised Uptake Value Ratio (SUVR) of 64Cu-ATSM binding in the dentate nuclei relative to the cerebral cortex estimated from the reconstructed PET scan after SUV equilibrium.
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Assessment method [1]
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0
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Timepoint [1]
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Single time-point
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Primary outcome [2]
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Standardised Uptake Value Ratio (SUVR) of 64Cu-ATSM binding in the brainstem relative to the cerebral cortex estimated from the reconstructed PET scan after SUV equilibrium.
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Assessment method [2]
321702
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Timepoint [2]
321702
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Single timepoint
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Secondary outcome [1]
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Scale for the Assessment and Rating of Ataxias (SARA)
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Assessment method [1]
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Timepoint [1]
375946
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Single timepoint
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Eligibility
Key inclusion criteria
- >18 years old
- Friedreich ataxia cohort: Genetically-confirmed diagnosis
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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?
Yes
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Key exclusion criteria
- Neurological illnesses (other than Friedreich ataxia in the clinical cohort)
- Psychiatric illnesses requiring current pharmacotherapy
- Concussion in the past 12 months, or any history of major traumatic brain injury
- Pregnancy
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Study design
Purpose
Screening
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Duration
Cross-sectional
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Selection
Case control
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Timing
Prospective
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Statistical methods / analysis
- Standardised uptake value ratios (SUVR) of the regions-of-interest (dentate nuclei and brainstem) will be calculated relative to the cerebral cortex.
- Between-group statistical inference will be undertaken using independent samples t-tests (or equivalent non-parametric Mann-Whitney U in the case of non-normality in the data).
- Linear correlations between SUVR values and clinical severity (SARA) will be undertaken using Pearson correlations (or equivalent non-parametric Spearman correlations in the event of non-normality in the data).
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/11/2019
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Actual
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Date of last participant enrolment
Anticipated
1/06/2020
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Actual
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Date of last data collection
Anticipated
1/06/2020
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Actual
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Sample size
Target
20
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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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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Monash University
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Address [1]
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Monash Biomedical Imaging
770 Blackburn Road
Monash University
Victoria, 3800
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Country [1]
304058
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Australia
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Primary sponsor type
University
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Name
Monash University
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Address
Monash Biomedical Imaging
770 Blackburn Road
Monash University
Victoria, 3800
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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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None
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Address [1]
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None
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Country [1]
304253
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Monash University Human Research and Ethics Committee
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Ethics committee address [1]
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Executive Officer Monash University Human Research Ethics Committee (MUHREC) Room 111, Chancellery Building E, 24 Sports Walk, Clayton Campus Research Office Monash University VIC 3800
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
304549
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Approval date [1]
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30/09/2019
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Ethics approval number [1]
304549
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18894
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Summary
Brief summary
Friedreich ataxia (FA) is a chronic, progressive, and terminal illness. Currently, there are no effective treatments and no sensitive biometrics of illness progression for FA. Oxidative stress has been proposed as a candidate molecular process that contributes to the underlying neuropathology, and/or reflects the cellular dysfunction underlying this disease. Measuring and tracking oxidative stress in the human brain using Positron Emission Tomography (PET) provides an opportunity for in vivo mechanistic characterisations disease in the human brain, and represents a novel and potentially sensitive approach to addressing the urgent need for pharmacodynamic and treatment monitoring biomarkers for use in clinical trials. The current study aims to investigate 64Cu-ATSM PET as a tool for imaging oxidative stress in the brains of individuals with FA.
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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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Dr Ian Harding
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Address
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Monash Biomedical Imaging
770 Blackburn Road
Monash University, VIC, 3800
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Country
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Australia
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Phone
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+61 3 9905 9283
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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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Ian Harding
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Address
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Monash Biomedical Imaging
770 Blackburn Road
Monash University, VIC, 3800
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Country
97347
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Australia
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Phone
97347
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+61 3 9905 9283
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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
97348
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Ian Harding
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Address
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Monash Biomedical Imaging
770 Blackburn Road
Monash University, VIC, 3800
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Country
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Australia
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Phone
97348
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+61 3 9905 9283
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Fax
97348
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Email
97348
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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
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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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