Osteoporosis Clinical Trial
Official title:
Frequency of Zoledronic Acid to Prevent Further Bone Loss in Osteoporotic Patients Requiring Androgen Deprivation Therapy for Prostate Cancer
The aim of this study is to determine if 3 monthly infusions of zoledronic acid, given over one year, improves the bone mineral density in osteoporotic patients undergoing androgen deprivation therapy for prostate cancer
Androgen Deprivation Therapy is the mainstay of treatment for advanced prostate cancer.
However they are associated with accelerated bone loss, osteoporosis and fractures. Previous
studied looking at the use of zoledronic acid have predominantly studied men with a normal
or osteopenic bone mineral density. However, it has been shown that upto 40% of men
presenting with prostate cancer have osteoporosis and it is these who are at most risk of
osteoporotic fractures. Our aim was to evaluate the efficiency of zoledronic acid in 2
groups of osteoporotic patients, those undergoing treatment with LHRH agonists and with
antiandrogens.Peripheral and axial bone densitometry will be used to measure percentage
changes in bone mineral density over 3 years. The first year with the patients on LHRH or
antiandrogen, the second year continuing with their androgen deprivation therapy and
zoledronic acid. Then bone mineral density will be measured one year following the last
infusion of zoledronic acid to ascertain the optimum frequency of administration.
The study will also involve monitoring serum and urine bone turnover markers.
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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