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Trial registered on ANZCTR


Registration number
ACTRN12607000128493
Ethics application status
Approved
Date submitted
9/02/2007
Date registered
14/02/2007
Date last updated
5/12/2016
Type of registration
Prospectively registered

Titles & IDs
Public title
The effect of low dose fluoride on bone
Scientific title
A randomized, double-blind, placebo-controlled, dose-finding study of the effects of sodium fluoride on bone turnover, bone density and bone histology in osteopenic post menopausal women.
Secondary ID [1] 262121 0
Nil
Universal Trial Number (UTN)
Trial acronym
FEAST
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Osteoporosis 1620 0
Condition category
Condition code
Musculoskeletal 1728 1728 0 0
Osteoporosis

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Subjects randomized to placebo or 1 of 3 treatment groups: sodium fluoride 2.5mg daily, per oral, 5mg daily per oral, 10mg daily per oral, for 1 year. No dosage increments Active and placebo tablets are identical in appearance
Intervention code [1] 1592 0
Treatment: Drugs
Comparator / control treatment
Matching placebo, per oral for 1 year
Control group
Placebo

Outcomes
Primary outcome [1] 2399 0
Change in lumbar spine bone mineral density (BMD
Timepoint [1] 2399 0
At 1 year
Secondary outcome [1] 4170 0
Change in hip BMD
Timepoint [1] 4170 0
At 1 year
Secondary outcome [2] 4171 0
Change in forearm BMD
Timepoint [2] 4171 0
At 1 year
Secondary outcome [3] 4172 0
Change in biochemical markers of bone turnover
Timepoint [3] 4172 0
At 1 year
Secondary outcome [4] 4173 0
Bone histology
Timepoint [4] 4173 0
At 1 year

Eligibility
Key inclusion criteria
Postmenopausal 5 yrs or more (menopause defined as at least 12 months since last period in woman aged > 45 yrs with intact uterus, or serum follicle stimluating hormone (FSH) > 50 IU/l in younger or hysterectomized woman)- Bone density T score less than -1.0 and greater than -2.5 at L1-L4 or Total Hip.- BMD T-score <-2.5 at lumbar spine or total hip, but participant is not a suitable candidate for, or has decided against taking, osteoporosis therapy
Minimum age
45 Years
Maximum age
Not stated
Sex
Females
Can healthy volunteers participate?
No
Key exclusion criteria
Medical Conditions- renal impairment (serum creatinine 120 µmol/L).- congestive heart failure- chronic liver disease.- untreated hypothyroidism or hyperthyroidism.- concurrent major systemic illness, including malignancy.- active major gastrointestinal disease.- metabolic bone diseases, or serum alkaline phosphatase (ALP) > 2x normal limit.- primary hyperparathyroidism. - Vitamin D insufficiency (25 hydroxyvitamin D [OHD] < 50nmol/L)Medications- use of oral glucocorticoid drugs equivalent to an average dose of prednisone 2.5 mg/day in the preceding 12 months- use of aminobisphosphonates within the past 2 years, or etidronate within the past 1 year- use of hormone replacement therapy within the last 12 months- use of other medication known to cause osteoporosis or interfere with bone metabolism.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Staff member enrolling subject unaware of treatment allocation, allocation concealment by central randomization
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Sequence generation by computer-generated random numbers
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
subjects and assessors are blinded
Phase
Phase 2
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
1/07/2009
Actual
30/06/2009
Date of last participant enrolment
Anticipated
Actual
31/03/2010
Date of last data collection
Anticipated
Actual
Sample size
Target
180
Accrual to date
Final
180
Recruitment outside Australia
Country [1] 482 0
New Zealand
State/province [1] 482 0

Funding & Sponsors
Funding source category [1] 1877 0
Government body
Name [1] 1877 0
Health Research Council of New Zealand
Country [1] 1877 0
New Zealand
Funding source category [2] 237233 0
Charities/Societies/Foundations
Name [2] 237233 0
Auckland Medical research Foundation
Country [2] 237233 0
New Zealand
Primary sponsor type
Individual
Name
Associate Professor Andrew Grey
Address
Department of Medicine
University of Auckland
Private Bag 92019
Auckland
Country
New Zealand
Secondary sponsor category [1] 1692 0
University
Name [1] 1692 0
University of Auckland
Address [1] 1692 0
Private Bag 92019
Auckland
Country [1] 1692 0
New Zealand

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 3502 0
Auckland-Northern X Regional Ethics Committee
Ethics committee address [1] 3502 0
Ethics committee country [1] 3502 0
New Zealand
Date submitted for ethics approval [1] 3502 0
Approval date [1] 3502 0
10/01/2007
Ethics approval number [1] 3502 0
NTX/06/12/152

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 27526 0
A/Prof Andrew Grey
Address 27526 0
Department of Medicine
university of Auckland
Private Bag 92019
Auckland
New Zealand
Country 27526 0
New Zealand
Phone 27526 0
+6493737599
Fax 27526 0
Email 27526 0
[email protected]
Contact person for public queries
Name 10781 0
Associate Professor Andrew Grey
Address 10781 0
Department of Medicine,
University of Auckland,
Auckland
Country 10781 0
New Zealand
Phone 10781 0
+64 9 3737599
Fax 10781 0
Email 10781 0
[email protected]
Contact person for scientific queries
Name 1709 0
Associate Professor Andrew Grey
Address 1709 0
Department of Medicine,
University of Auckland,
Auckland
Country 1709 0
New Zealand
Phone 1709 0
+64 9 3737599
Fax 1709 0
Email 1709 0
[email protected]

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
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