This study will evaluate the effects of zoledronic acid 5 mg infusion on BMD and biochemical markers of bone in post-menopausal osteoporotic patients aged between 50-65.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
118
Novartis Investigational site
Ankara, Turkey (Türkiye)
Novartis Investigative site
Antalya, Turkey (Türkiye)
Novartis Investigational site
Istanbul, Turkey (Türkiye)
Novartis Investigative site
Izmir, Turkey (Türkiye)
Efficacy - BMD
Time frame: 1 year
Efficacy - Biochemical markers
Time frame: 6 months
Safety - Rate of adverse events and serious adverse events
Time frame: 6 months
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Novartis Investigative site
Kayseri, Turkey (Türkiye)
Novartis Investigative site
Konya, Turkey (Türkiye)