CompletedPhase 4ACTRN12605000278639

The Duration of Action of Zoledronate study

A three year randomised, double-blind, placebo-controlled trial to determine the duration of effect of zoledronate on bone turnover markers and on bone density in post menopausal women with osteopenia.


Sponsor

Professor I Reid

Enrollment

50 participants

Start Date

Apr 26, 2005

Study Type

Interventional

Conditions

Summary

This is a 3 year study designed to determine the duration of action of a single dose of intravenous zoledronate.


Eligibility

Sex: FemalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying the Duration of Action of Zoledronate study. You may be eligible if you are women aged 18 and older who postmenopausal 5 yrs or more, bone density T score between -1.0 and -2.0 at lumbar spine or total hip. People with renal impairment (serum creatinine >0.15 mmol/l), chronic liver disease, untreated hypothyroidism or hyperthyroidism may not be able to participate. Participation may involve medical tests, study visits, and follow-up appointments.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

One infusion of 5mg intravenous zoledronate.

One infusion of 5mg intravenous zoledronate.


Locations(1)

New Zealand

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ACTRN12605000278639