It is the aim of this clinical study to evaluate the skeletal-related event rate and tolerability of zoledronic acid in patients with prostate cancer patients and bone metastases.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
284
Rate of skeletal complications
Time frame: 3 months
Time to first skeletal complication
Time frame: 3 months
Bone pain
Time frame: 3 months
Patients´ satisfaction with treatment
Time frame: 3 months
Bone turnover parameters
Time frame: 3 months
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