It is the aim of this multicentric clinical study to assess the efficacy and tolerability of zoledronic acid in combination with radiotherapy in patients with advanced osteolytic bone lesions in terms of the reduction of pain and analgesic consumption.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
75
Novartis Investigative Site
Herne, Germany
Pain reduction
Time frame: weekly assessments during 48 weeks
Time to pain reduction
Time frame: weeks 0, 12, 24, 36, 48 and 60
Duration of pain reduction
Time frame: weeks 0, 12, 24, 36, 48 and 60
Quality of life
Time frame: weeks 0, 12, 24, 36, 48 and 60
Changes in parameters of bone turnover
Time frame: weeks 0, 12, 24, 36, 48 and 60
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