Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12612000270819
Ethics application status
Approved
Date submitted
5/03/2012
Date registered
6/03/2012
Date last updated
30/08/2024
Date data sharing statement initially provided
30/08/2024
Type of registration
Prospectively registered

Titles & IDs
Public title
Zoledronate and fracture prevention in early postmenopausal women
Scientific title
Efficacy of very infrequent zoledronic acid on vertebral fractures and bone mineral density in early postmenopausal women
Secondary ID [1] 280075 0
Nil
Universal Trial Number (UTN)
Nil
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Osteoporosis 285984 0
Condition category
Condition code
Musculoskeletal 286174 286174 0 0
Osteoporosis

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Arm 1: Intravenous infusion of 5mg zoledronic acid at baseline and an intravenous infusion of placebo (saline solution) at 5 years. (Total of two infusions during study)
Arm 2: Intravenous infusion of 5mg zoledronic acid at baseline and 5 years. (Total of two infusions during study)
Intervention code [1] 284397 0
Prevention
Intervention code [2] 284408 0
Treatment: Drugs
Comparator / control treatment
Arm 3: Intravenous infusion of placebo (normal saline) at baseline and 5 years. (Total of two infusions during study)
Control group
Placebo

Outcomes
Primary outcome [1] 286640 0
New morphometric vertebral fractures since baseline assessed using thoracic and lumbar spine plain x-rays
Timepoint [1] 286640 0
Thoracic and spinal x-rays will be taken at baseline, 5 years, and 10 years in all participants.
Secondary outcome [1] 296346 0
Change in bone mineral density from baseline measured at the spine, hip and whole body with dual enery x-ray absorptiometry
Timepoint [1] 296346 0
Bone density will be measured at baseline, 5 years and 10 years in all participants, and in a subset of 225 participants at 2.5 years and 7.5 years.
Secondary outcome [2] 296347 0
Incidence of any, fragility, and major osteoporotic fractures assessed using plain x-rays, CT or MRI imaging.
Timepoint [2] 296347 0
10 years
Secondary outcome [3] 296348 0
Change in bone turnover markers since baseline
Timepoint [3] 296348 0
Bone turnover markers will be measured in a subset of 225 participants at baseline, 2.5 years, 5 years, 7.5 years and 10 years
Secondary outcome [4] 296349 0
Equivalence of 5mg zoledronate administered using two different dosing intervals (either 5mg at baseline or 5mg at baseline and 5 years) in preventing new morphometric vertebral fractures since baseline assessed using thoracic and lumbar spine plain x-rays
Timepoint [4] 296349 0
Thoracic and spinal x-rays will be taken at baseline, 5 years, and 10 years in all participants.
Secondary outcome [5] 296383 0
Adverse events (including the expected adverse event of acute phase reactions)
Timepoint [5] 296383 0
Medical history and adverse events will be assessed by interview at baseline, and every 6 months until 10 years. Assessments will be at a clinic visit at baseline, 5 years and 10 years, and by phone or email contact at other timepoints.

Eligibility
Key inclusion criteria
Postmenopausal women aged 50-60 years.
Bone mineral density T score at the lumbar spine, femoral neck or total hip < 0
Minimum age
50 Years
Maximum age
60 Years
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Bone mineral density T score <-2.5 at the total hip, femoral neck or lumbar spine.
Renal impairment (estimated glomerular filtration rate > 45 ml/min).
Untreated hypothyroidism or hyperthyroidism.
Chronic liver disease.
Concurrent major systemic illness, including malignancy.
Active major gastrointestinal disease.
Metabolic bone diseases.
Previous fragility fracture of the hip or spine.
Current or past use of bisphosphonate therapy within 12 months, or past zoledronic acid use.
Use of oral glucocorticoid drugs equivalent to an average dose of at least prednisone 2.5mg/day during the preceding 6 months.
Use of hormone replacement therapy within 12 months

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Subject numbers will be allocated by personnel based in a different building and having no contact with study subjects. Infusions of study medication (zoledronate or placebo) will be prepared by a staff member who has no contact with the study subjects and no role in any other study procedures including assessments of end-points. All personnel having contact with study subjects and the subjects themselves will be blinded to treatment allocation.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer-generated random numbers in variable blocks
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
Intervention assignment
Parallel
Other design features
Phase
Phase 4
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
1/05/2012
Actual
22/05/2012
Date of last participant enrolment
Anticipated
Actual
5/08/2013
Date of last data collection
Anticipated
Actual
25/10/2023
Sample size
Target
1050
Accrual to date
Final
1054
Recruitment outside Australia
Country [1] 4183 0
New Zealand
State/province [1] 4183 0

Funding & Sponsors
Funding source category [1] 284830 0
Government body
Name [1] 284830 0
Health Research Council of New Zealand
Country [1] 284830 0
New Zealand
Primary sponsor type
Individual
Name
Dr Mark Bolland
Address
Bone and Joint Research Group,
Department of Medicine,
University of Auckland,
85 Park Road, Grafton
Private Bag 92019,
Auckland, 1142
Country
New Zealand
Secondary sponsor category [1] 283708 0
None
Name [1] 283708 0
Address [1] 283708 0
Country [1] 283708 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 286819 0
Northern X Regional Ethics Committee
Ethics committee address [1] 286819 0
Ethics committee country [1] 286819 0
New Zealand
Date submitted for ethics approval [1] 286819 0
Approval date [1] 286819 0
07/12/2011
Ethics approval number [1] 286819 0
NTX/11/11/097

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

Contacts
Principal investigator
Name 33866 0
A/Prof Mark Bolland
Address 33866 0
Bone and Joint Research Group, Department of Medicine, University of Auckland, 85 Park Road, Grafton Private Bag 92019, Auckland, 1142
Country 33866 0
New Zealand
Phone 33866 0
6493737599
Fax 33866 0
Email 33866 0
[email protected]
Contact person for public queries
Name 17113 0
Dr Anne Horne
Address 17113 0
Bone and Joint Research Group,
Department of Medicine,
University of Auckland,
85 Park Road, Grafton
Private Bag 92019,
Auckland, 1142
Country 17113 0
New Zealand
Phone 17113 0
64 9 9239787
Fax 17113 0
64 9 3072865
Email 17113 0
[email protected]
Contact person for scientific queries
Name 8041 0
Mark Bolland
Address 8041 0
Bone and Joint Research Group,
Department of Medicine,
University of Auckland,
85 Park Road, Grafton
Private Bag 92019,
Auckland, 1142
Country 8041 0
New Zealand
Phone 8041 0
64 9 3737599
Fax 8041 0
64 9 3737677
Email 8041 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
De-identified data underpinning published results
When will data be available (start and end dates)?
12 months after relevant publication with no end date determined
Available to whom?
Researchers who provided a protocol that is methodologically sound
Available for what types of analyses?
Analyses specified in the approved protocol
How or where can data be obtained?
By contacting the principal investigator ([email protected])


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
SourceTitleYear of PublicationDOI
Dimensions AIIntravenous zoledronate for osteoporosis: less might be more2016https://doi.org/10.1177/1759720x16650866
Dimensions AIBone Mineral Density and Bone Turnover 10 Years After a Single 5 mg Dose or Two 5-Yearly Lower Doses of Zoledronate in Osteopenic Older Women: An Open-Label Extension of a Randomized Controlled Trial2020https://doi.org/10.1002/jbmr.4453
N.B. These documents automatically identified may not have been verified by the study sponsor.