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Calcium Fracture Study

Anti-fracture efficacy of calcium supplementation in normal postmenopausal women

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12605000242628
Enrollment
1500
Registered
2005-08-31
Start date
1998-03-17
Completion date
2000-08-09
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This is a 5 year study designed to determine whether a 1g calcium supplement daily prevents symptomatic fractures.

Interventions

Daily 1g calcium (as the citrate) over 5 years.

Sponsors

Professor I Reid
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Females >5 years postmenopausal and aged >55 years with life-expectancy >5 years.

Exclusion criteria

Renal impairment (serum creatinine > 0.2mmol/l), Untreated hypo- or hyperthyroidism, Active liver disease, Serum 25-hydroxyvitamin D < 14 ng/ml, Concurrent major systemic disease, including malignancy, Metabolic bone disease, Regular use of hormone replacement therapy within the previous 1 year, Regular use of sodium fluoride in a dose greater than or equal to 20mg per day in the previous 1 year, Regular use of anabolic steroid preparations in the previous 1 year, Treatment with bisphosphonates in the previous 1 year, Current treatment with glucocorticoid drugs, Calciferol supplements in doses >1000 iu/day or 50,000 iu/month, Lumbar spine bone density < mean-2.0 SD for age-appropriate data.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026