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Trial registered on ANZCTR
Registration number
ACTRN12606000458538
Ethics application status
Approved
Date submitted
26/10/2006
Date registered
31/10/2006
Date last updated
31/10/2006
Type of registration
Prospectively registered
Titles & IDs
Public title
Comparison of the effects of two marketed calcium preparations on reducing serum markers of bone resorption in post menopausal women
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Scientific title
Comparison of the effects of two marketed Calcium preparations on reducing serum markers of bone resorption in post menopausal women
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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:
Healthy volunteers (post menopausal women)
1433
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Condition category
Condition code
Reproductive Health and Childbirth
1529
1529
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0
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Menstruation and menopause
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A cross over trial using Calsup (calcium carbonate) 1000 mg and Citracal (calcium citrate) 500mg given as single doses orally, one week apart following base line serum tests.
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Intervention code [1]
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Prevention
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Comparator / control treatment
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Control group
Active
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Outcomes
Primary outcome [1]
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Auppression of bone resorption markers in serum
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Assessment method [1]
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Timepoint [1]
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About 12 hours after each dose
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Secondary outcome [1]
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Serum calcium level
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Assessment method [1]
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Timepoint [1]
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Measured as a base line before intervention and then 12 hours after each intervention.
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Secondary outcome [2]
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Serum PTH (parathyroid hormone) level
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Assessment method [2]
3654
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Timepoint [2]
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Measured as a base line before intervention and then 12 hours after each intervention.
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Eligibility
Key inclusion criteria
Post menopausal (menopause within last 5 years)
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Minimum age
50
Years
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Maximum age
55
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. renal failure, intake of calcium supplements, hypercalcaemiaany bone disorder.
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Study design
Purpose of the study
Prevention
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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)
sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
simple randomisation by using a randomisation table created by a computer software program
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Crossover
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Other design features
subjects and assesor are blinded
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Phase
Phase 1
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/11/2006
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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
25
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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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Other
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Name [1]
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Department of Clinical Biochemistry, Institute of Medical and Veterinary Science, Adelaide
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Address [1]
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Country [1]
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Australia
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Primary sponsor type
Charities/Societies/Foundations
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Name
Institute of Medical and Veterinary Science, Frome road, Adelaide, SA 5000
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Address
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Country
Australia
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Secondary sponsor category [1]
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Hospital
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Name [1]
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Royal Adelaide Hospital
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Address [1]
1471
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Country [1]
1471
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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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Royal Adelaide Hospital Research Ethics Committee
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Ethics committee address [1]
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
3109
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Approval date [1]
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17/10/2006
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Ethics approval number [1]
3109
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060918
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Summary
Brief summary
Calcium supplementation has been shown to reduce the incidence of osteoporosis and related fractures. Currently Calsup (calcium carbonate) is marketed widely in Australia. This study is to compare the effects of Calsup with a newer calcium supplement, Citracal (Calcium citrate) on reducing serum markers of bone resorption. The hypothesis is that citracal may be equally effective in smaller doses and would have less side effects.
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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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Dr Devika Grasby
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Address
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Department of Clinical Biochemistry
Institute of Medical and Veterinary Science
Frome Road
Adelaide SA 5000
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Country
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Australia
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Phone
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+61 8 82223611
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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
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Dr Devika Grasby
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Address
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Department of Clinical Biochemistry
Institute of Medical and Veterinary Science
Frome Road
Adelaide SA 5000
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Country
1537
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Australia
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Phone
1537
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+61 8 82223611
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Fax
1537
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Email
1537
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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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