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Trial registered on ANZCTR
Registration number
ACTRN12607000345482
Ethics application status
Approved
Date submitted
26/06/2007
Date registered
26/06/2007
Date last updated
14/07/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
The potential of selenium supplements provided as selenium-enriched dairy protein or yeast selenium to improve selenium status
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Scientific title
The potential of selenium supplements provided as selenium-enriched dairy protein or yeast selenium to improve selenium status
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Universal Trial Number (UTN)
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Trial acronym
nil
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Plasma selenium concentration
Levels of biomarkers in rectal epithelium
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Condition category
Condition code
Diet and Nutrition
1991
1991
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0
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Other diet and nutrition disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
It is proposed to evaluate a selenised dairy product (Tatura Bio Se®, TMI Victoria) in a human intervention study with regard to its safety and influence on selenium status, using plasma and rectal biomarkers.
A group of >50 year old volunteers considered at-risk for colon cancer by virtue of age and/or other standard risk factors.
Particpants will commence with a wash out period of 2-4 wks instructing them not to add selenium products to their diet
10 participants will be allocated Se Milk Protein Concentrate 150µg/d and a different group of 10 will be allocated Selplex 150µg/d at the same time i.e to run in parallel
Each participant will undertake a follow on wash out period of 6 weeks.
Blood samples will be taken every 2 weeks throughout the intervention and wash out periods
Rectal pinch biopsies will be performed for bowel tissue samples at the beginning and end of each intervention and at the end of the follow-on washout period.
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Intervention code [1]
1852
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Prevention
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Comparator / control treatment
It will be compared for its efficacy and bioavailability with a selenium yeast (Sel-plex ?,Alltech) product.
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Control group
Active
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Outcomes
Primary outcome [1]
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Level of plasma glutathione peroxidase (GSPx), plasma selenium concentration & plasma selenoprotein P
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Assessment method [1]
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Timepoint [1]
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Taken at fortnightly intervals throughout the study
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Primary outcome [2]
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Level of biomarkers in rectal epithelium including selected endpoints from selenium concentration and Glutathione Peroxidase (GSPx)
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Assessment method [2]
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Timepoint [2]
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Taken at commencement & end of intervention (week 0 & week 6) & at end of 6wk follow on/wash out period
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Secondary outcome [1]
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Level of biomarkers in rectal epithelium. They include selenium concentration and thioredoxin reductase and glutathione peroxidase activities, and histologically: PCNA cell proliferation and apoptosis rates, and p53 immunohistochemical staining.
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Assessment method [1]
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Timepoint [1]
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Taken at commencement & end of intervention (week 0 & week 6) & at end of 6wk follow on/wash out period
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Secondary outcome [2]
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Level of biomarkers in blood taken, including plasma Se, GSPx & selenoprotein P.
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Assessment method [2]
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Timepoint [2]
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At fortnightly intervals throughout the study.
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Eligibility
Key inclusion criteria
Healthy, with no active bowel disease, orWith a previous history of adenoma removal >6 months ago, With plasma selenium at or below 100 µg/dL. (to ensure that people with a High background selenium status are not included in the study),
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Minimum age
50
Years
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Maximum age
Not stated
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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
Any allergy or intolerance to milk/dairy productsPlasma Se above the 95th percentile of the current population (i.e. >100µg/dL)Evidence of any active mucosal bowel disease, eg colitis, or of malabsorption.With no evidence of any other active clinical disease precluding participation in the study.
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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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
Parallel
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Bio-availability
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
20/11/2007
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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
20
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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Geoffrey Gardiner Dairy Foundation Ltd (GGDF)
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Address [1]
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Level 1 84 William Street
Melbourne VIC 3000
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Professor Graeme Young MD, FRACP
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Address
Department of Medicine (Gastroenterology)
Flinders University
Flinders Medical Centre
Bedford Park SA 5042
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Professor Graeme McIntosh BVSc PhD,
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Address [1]
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9A Serpentine Rd.,
Belair, South Australia 5052
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Country [1]
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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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Flinders Medical Centre-Flinders Clinical Drug Trials Committee & Flinders Clinical Research & Ethics Committee
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Ethics committee address [1]
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Bedford Park SA 5042
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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Approval date [1]
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24/09/2007
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Ethics approval number [1]
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214/067
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Summary
Brief summary
It is proposed to evaluate a selenised dairy product with regard to its safety and influence on selenium status, using plasma and rectal biomarkers. It will be compared for its efficacy & bioavailability with a selenium yeast product.
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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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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Ms Jane Upton RN
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Address
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Department of Gastroenterology
Flinders Medical Centre
Bedford Park SA 5042
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Country
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Australia
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Phone
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+61 8 82046071
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Fax
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+61 8 82046330
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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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Professor Graeme McIntosh BVSc PhD,
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Address
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Department of Gastroenterology
Flinders Medical Centre,
Bedford Park, SA 5042
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Country
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Australia
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Phone
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+61 8 82044964
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Fax
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+61 8 82043943
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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.
Download to PDF