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Trial registered on ANZCTR
Registration number
ACTRN12611001271998
Ethics application status
Approved
Date submitted
8/12/2011
Date registered
12/12/2011
Date last updated
19/08/2019
Date data sharing statement initially provided
19/08/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
The Impact of Micronutrients on Gene Expression in Prostate Cancer: Lycopene
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Scientific title
The Impact of Micronutrients on Gene Expression in Prostate Cancer: Lycopene
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Secondary ID [1]
273565
0
Nil
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Universal Trial Number (UTN)
U1111-1126-3180
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Trial acronym
ImoGEX(TM)-PC-Lyc
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Prostate cancer
279362
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Condition category
Condition code
Cancer
285549
285549
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0
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Prostate
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Lycopene - oral supplement 3 times daily - 15-90mg for 6-10 weeks; differs on a case-by-case basis as determined by clinician
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Intervention code [1]
283867
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Treatment: Other
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Comparator / control treatment
Nil
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
286112
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Global gene expression via blood and tissue analysis
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Assessment method [1]
286112
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Timepoint [1]
286112
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Baseline - post-prostatectomy
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Secondary outcome [1]
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A range of markers measured using blood analysis, including: full blood count, PSA, lipids, IGF-1, IGFBP3
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Assessment method [1]
295174
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Timepoint [1]
295174
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Baseline - post-prostatectomy
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Eligibility
Key inclusion criteria
(1) Age 35-80 years
(2) Non-smoker
(3) Patients with a diagnosis of clinically localised prostate cancer who are scheduled to undergo radical prostatectomy in 6-8 weeks
(4) Normal liver function tests, as verification that the tumour is localized to the prostate gland
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Minimum age
35
Years
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Maximum age
80
Years
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
(1) No diagnosis of prostate cancer
(2) Body mass index <18.5kg/m2 (underweight) or >35kg/m2 (obese – class II)
(3) Current infection
(4) Prior therapy for prostate cancer (e.g. chemotherapy; radiation therapy; hormonal therapy)
(5) Current consumption of testosterone replacement medicines
(6) Current consumption of 5-alpha-reductase inhibitors
(7) Consumption of other herbal or nutritional supplements, apart from a single multi-vitamin tablet
(8) Inability to provide informed consent due to diminished understanding or comprehension, or a language other than English spoken and an interpreter unavailable
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Study design
Purpose of the study
Prevention
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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)
All patients receive the treatment
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
All patients receive the treatment
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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
Patients serve as their own control
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Phase
Phase 1 / Phase 2
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Withdrawn
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Reason for early stopping/withdrawal
Other reasons/comments
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Other reasons
An appropriate trial product could not be sourced for this study (lycopene), so a different study in the same area utilising a different intervention was registered with ANZCTR.
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Date of first participant enrolment
Anticipated
1/02/2012
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
24
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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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Funding & Sponsors
Funding source category [1]
284350
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Charities/Societies/Foundations
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Name [1]
284350
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Sanofi Aventis Prostate Cancer Research Award
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Address [1]
284350
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Clinical Oncological Society of Australia
Level 1, 120 Chalmers Street
Surry Hills NSW 2010
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Country [1]
284350
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Australia
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Primary sponsor type
University
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Name
University of Queensland
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Address
St Lucia
Brisbane QLD 4072
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Country
Australia
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Secondary sponsor category [1]
283288
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None
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Name [1]
283288
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Nil
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Address [1]
283288
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Nil
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Country [1]
283288
0
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Other collaborator category [1]
260381
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Other Collaborative groups
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Name [1]
260381
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Mater Medical Research Institute
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Address [1]
260381
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Level 3, Aubigny Place
Raymond Terrace
South Brisbane QLD 4101
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Country [1]
260381
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Australia
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Other collaborator category [2]
260382
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University
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Name [2]
260382
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Diamantina Institute, The University of Queensland
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Address [2]
260382
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R-Wing
Princess Alexandra Hospital
Ipswich Road, Woolloongabba QLD 4102
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Country [2]
260382
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Australia
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Other collaborator category [3]
260383
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Other Collaborative groups
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Name [3]
260383
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Translational Research Institute
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Address [3]
260383
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Princess Alexandra Hospital
Ipswich Road, Woolloongabba QLD 4102
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Country [3]
260383
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
286310
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Greenslopes Private Hospital Human Research Ethics Committee
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Ethics committee address [1]
286310
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Greenslopes Private Hospital Newdgate Street Greenslopes QLD 4120
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Ethics committee country [1]
286310
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Australia
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Date submitted for ethics approval [1]
286310
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Approval date [1]
286310
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21/09/2011
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Ethics approval number [1]
286310
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11/40
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Ethics committee name [2]
286311
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Mater Health Services Human Research Ethics Committee
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Ethics committee address [2]
286311
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Mater Misericordiae Health Services Brisbane Ltd Raymond Terrace South Brisbane QLD 4101
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Ethics committee country [2]
286311
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Australia
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Date submitted for ethics approval [2]
286311
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06/09/2011
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Approval date [2]
286311
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Ethics approval number [2]
286311
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1839P
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Summary
Brief summary
The purpose of this study is to conduct a small, translational research trial in a group of men with prostate cancer, to determine the whole-genome effects of lycopene supplementation.
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Trial website
Nil
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Trial related presentations / publications
Nil
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Public notes
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Contacts
Principal investigator
Name
33515
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Dr Olivia Wright
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Address
33515
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School of Human Movement and Nutrition Sciences
The University of Queensland
QLD 4072
Australia
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Country
33515
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Australia
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Phone
33515
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+61 7 33656669
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Fax
33515
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Email
33515
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[email protected]
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Contact person for public queries
Name
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Dr Olivia Wright
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Address
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School of Human Movement Studies
Level 5, Connell Building
The University of Queensland
St Lucia QLD 4072
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Country
16762
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Australia
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Phone
16762
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+61 7 3346 7768
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Fax
16762
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+61 7 3365 6877
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Email
16762
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[email protected]
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Contact person for scientific queries
Name
7690
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Dr Olivia Wright
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Address
7690
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School of Human Movement Studies
Level 5, Connell Building
The University of Queensland
St Lucia QLD 4072
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Country
7690
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Australia
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Phone
7690
0
+61 7 3346 7768
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Fax
7690
0
+61 7 3365 6877
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Email
7690
0
[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
The study as it was first registered has been withdrawn.
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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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