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Trial registered on ANZCTR
Registration number
ACTRN12605000368639
Ethics application status
Approved
Date submitted
23/08/2005
Date registered
13/09/2005
Date last updated
13/09/2005
Type of registration
Retrospectively registered
Titles & IDs
Public title
Effect of iodine and selenium intervention on the thyroid status of older New Zealanders
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Scientific title
Effect of iodine and selenium intervention on the thyroid status of older New Zealanders
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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:
Selenium, Iodine and Thyroid Status
463
0
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Condition category
Condition code
Metabolic and Endocrine
540
540
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0
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Normal metabolism and endocrine development and function
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants will be randomised into one of four treatment groups & given a supplement containing either; selenium, iodine, selenium & iodine or placebo. Participants take one supplement daily for 12 weeks. Selenium, iodine and thryoid status of participants will be measured at 5 time point over the intervention.
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Intervention code [1]
227
0
None
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Comparator / control treatment
Placebo
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Control group
Placebo
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Outcomes
Primary outcome [1]
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To determine the effects of a 12 week supplementation with iodine and selenium on thyroid status
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Assessment method [1]
631
0
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Timepoint [1]
631
0
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Secondary outcome [1]
1304
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To investigate interactions between selenium and thyroid status
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Assessment method [1]
1304
0
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Timepoint [1]
1304
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At 5 time points over a 12 week period.
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Secondary outcome [2]
1305
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To determine the effects of iodine supplementation, with or without selenium, on throid metabolism as measured by the ratio of the active hormone T3 to the inactive hormone T4.
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Assessment method [2]
1305
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Timepoint [2]
1305
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At 5 time points over a 12 week period.
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Eligibility
Key inclusion criteria
Plasma Selenium <100ugLPersons not institutionalisedAmbulatoryGood Health with no serious medical illnesses
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Minimum age
65
Years
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Maximum age
80
Years
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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
Institutionalised. Plasma Se >100ugL. Serious Medical Illness
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
A statistician randomly allocated participants to one of the four groups (A, B, C or D). Participants will be given a tablet bottle containing either tablets A, B, C or D, none of the researchers conducting the study know what supplement type each letter signifies-One person within our department holds the 'code breaker' for the study which tells us what supplement type each letter corresponds to.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Statistician used block randomisation & computer software to generate the random allocation sequence
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Masking / blinding
Blinded (masking 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
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/08/2005
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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
100
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
143
0
New Zealand
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State/province [1]
143
0
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Funding & Sponsors
Funding source category [1]
598
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Charities/Societies/Foundations
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Name [1]
598
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University Melb.Dept. Gen Practice
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Address [1]
598
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Country [1]
598
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New Zealand
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Primary sponsor type
University
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Name
University of Otago, Dunedin, New Zealand
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Address
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Country
New Zealand
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Secondary sponsor category [1]
487
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None
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Name [1]
487
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nil
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Address [1]
487
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Country [1]
487
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1696
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University of Otago Human Ethics Committee
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Ethics committee address [1]
1696
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Ethics committee country [1]
1696
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New Zealand
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Date submitted for ethics approval [1]
1696
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Approval date [1]
1696
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Ethics approval number [1]
1696
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Summary
Brief summary
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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
35629
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Address
35629
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Country
35629
0
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Phone
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Fax
35629
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Email
35629
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Contact person for public queries
Name
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Jenny Campbell
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Address
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C/- Department of Human Nutrition University of Otago
Union St
PO Box 56
Dunedin 9007
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Country
9416
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New Zealand
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Phone
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+64 3 4795673
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Fax
9416
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Email
9416
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[email protected]
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Contact person for scientific queries
Name
344
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Associate Professor Christine Thomson
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Address
344
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C/- Department of Human Nutrition University of Otago
Union St
PO Box 56
Dunedin 9007
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Country
344
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New Zealand
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Phone
344
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+64 3 4797943
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Fax
344
0
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Email
344
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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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