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Trial registered on ANZCTR
Registration number
ACTRN12618000386235
Ethics application status
Approved
Date submitted
6/02/2018
Date registered
15/03/2018
Date last updated
15/03/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Establishing an Australian reference range for patients with Parkinson’s disease
and healthy controls with F-DOPA Positron Emission Tomography.
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Scientific title
Establishing an Australian reference range for striatal binding in patients with Parkinson’s disease and healthy controls with 6-[18F]fluoro-L-3,4-dihydroxyphenylalanine (F-DOPA) PET.
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Secondary ID [1]
293972
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None
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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:
Parkinson's disease
306484
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Condition category
Condition code
Neurological
305581
305581
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0
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Parkinson's disease
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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
We propose to perform F-DOPA Positron Emission Tomography (PET) scans in 20 participants with typical clinical features of Parkinson’s disease (PD). Images will be compared to their standard care Magnetic Resonance Imaging (MRI) scans to identify brain structures. Previous MRI scans, performed within the last 12 months, will be selected for comparison to PET scans. All participants will be monitored for the duration of the PET scan appointment (approximately 4 hours). No additional follow-up will be performed on this study.
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Intervention code [1]
300243
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Not applicable
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Comparator / control treatment
We propose to perform one F-DOPA Positron Emission Tomography (PET) scan and one Magnetic Resonance Imaging (MRI) scan on 10 healthy volunteer controls. MRI scans will be used to identify brain structures. The F-DOPA PET scan will be performed within 4 months of the MRI scan. Participants will be observed for 4 hours while attending the PET scan appointment and 1 hour during the MRI scan appointment. No additional follow-up will be performed on this study.
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Control group
Active
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Outcomes
Primary outcome [1]
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Difference in the striatoccipital ratio (SOR) between health controls and Parkinson's disease (PD) subjects by assessment of FDOPA brain activity on PET scans.
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Assessment method [1]
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Timepoint [1]
304703
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At completion of all subject imaging at the end of the study.
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Secondary outcome [1]
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Estimate the diagnostic yield (sensitivity and specificity) of F-DOPA PET-CT scans in differentiating between normal healthy subjects and subjects with early and advanced-stage Parkinson's disease by assessing brain structures on MRI and brain activity on the FDOPA PET scan.
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Assessment method [1]
342857
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Timepoint [1]
342857
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At completion of all subject imaging at the end of the study.
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Secondary outcome [2]
343448
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We will record any adverse events that occur in any group during the PET imaging process to assist in the assessment of the safety of F-DOPA PET imaging, although no adverse events from this procedure are anticipated..
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Assessment method [2]
343448
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Timepoint [2]
343448
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At completion of all participant imaging.
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Eligibility
Key inclusion criteria
Parkinson's disease: based on the UK Brain bank clinical criteria and a Hoehn and
Yahr score of 2.5 or less (early PD) or 3.0 or more (late PD).
Normal controls: aged matched individuals with no historical or clinical evidence of
any neurological disorder.
Greater than 18 years of age
Able to undertake PET imaging
Able to provide written informed consent
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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
Pregnancy
Less than 18 years of age
Medical contraindication to PET or MRI imaging
Patients with concurrent psychiatric disorders, signs of severe cognitive deterioration and severe cardiovascular comorbidity.
Cognitive impairment considered to impair the ability to give written informed consent in the opinion of the treating clinician
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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
Based on previously published data from Groningen University Hospital, the mean contralateral striato-occipital ratio (SOR) was 2.69 (SD 0.27) in healthy controls compared with a mean of 2.09 (SD 0.14) in earlystage Parkinson's disease (PD). Assuming a difference of a similar magnitude in our participant population, we estimate a minimum sample size of 4 subjects to demonstrate a statistically significant difference in contralateral SOR between healthy controls and early-stage PD subjects with a power of 0.99 and type I error rate of 5% (2 sample, 1-sided t-test).
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
20/03/2018
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Actual
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Date of last participant enrolment
Anticipated
10/03/2020
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Actual
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Date of last data collection
Anticipated
10/03/2020
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Actual
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Sample size
Target
30
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
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Sir Charles Gairdner Hospital - Nedlands
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Recruitment postcode(s) [1]
18787
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6009 - Nedlands
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Recruitment postcode(s) [2]
18788
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6000 - Perth
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Funding & Sponsors
Funding source category [1]
298604
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Charities/Societies/Foundations
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Name [1]
298604
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Australian and New Zealand Socieity of Nuclear Medicine LTD
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Address [1]
298604
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PO Box 6178, Vermont South,
VIC 3133
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Country [1]
298604
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Australia
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Primary sponsor type
Hospital
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Name
Sir Charles Gairdner Hospital
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Address
Hospital Avenue, Nedlands, Western Australia 6009
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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]
297763
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Address [1]
297763
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Country [1]
297763
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
299564
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Sir Charles Gairdner and Osborne Park Health Care Group
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Ethics committee address [1]
299564
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Hospital Avenue, Nedlands, Western Australia 6009
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Ethics committee country [1]
299564
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Australia
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Date submitted for ethics approval [1]
299564
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28/03/2017
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Approval date [1]
299564
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29/05/2017
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Ethics approval number [1]
299564
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RGS0000000183
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Summary
Brief summary
We propose to perform F-DOPA PET scans in 10 healthy volunteers and 20 participants with typical features of Parkinson’s disease (PD). Each will undergo an F-DOPA PET/CT scan. The healthy participants will also undergo an MRI scan to identify brain structures. Analysis of these scans will allow us to estimate how sensitive this PET scan is in discriminating between Parkinson’s disease and healthy people with no evidence of Parkinson’s disease. The collected data will assist in establishing Australian reference ranges which will assist in future analysis of these PET scans for patients with Parkinson’s disease.
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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 Nelson Loh
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Address
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Charles Gairdner Hospital
WA PET Service/ Department of Nuclear Medicine
G Block, level 1
Hospital Ave
Nedlands, WA, 6009
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Country
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Australia
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Phone
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+61 08 6457 2322
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Fax
80854
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+61 08 6457 7422
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Email
80854
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[email protected]
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Contact person for public queries
Name
80855
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Elaine Campbell
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Address
80855
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Charles Gairdner Hospital
WA PET Service/ Department of Nuclear Medicine
G Block, level 1
Hospital Ave
Nedlands, WA, 6009
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Country
80855
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Australia
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Phone
80855
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+61 08 6457 2322
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Fax
80855
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+61 08 6457 7422
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Email
80855
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[email protected]
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Contact person for scientific queries
Name
80856
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Elaine Campbell
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Address
80856
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Charles Gairdner Hospital
WA PET Service/ Department of Nuclear Medicine
G Block, level 1
Hospital Ave
Nedlands, WA, 6009
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Country
80856
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Australia
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Phone
80856
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+61 08 6457 2322
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Fax
80856
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Email
80856
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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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