The primary objective of this study is to assess the impact of physician's reinforcement using bone marker data on the subject's compliance (at least 50% drug taken) and persistence on treatment after one year in postmenopausal osteoporotic women.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
To assess the impact of physician's reinforcement using bone marker data on the treatment adherence of women with PMO.
Time frame: collected at week 10 and 22
to establish the profile of the unrecognized osteoporotic woman (PVD-, RF-) using a risk factor questionnaire for osteoporosis
Time frame: During the study conduct
to assess the decrease of type I collagen breakdown products(urinary NTX and serum CTX)
Time frame: after 10 and 22 weeks of treatment
To assess the change in BMD of both total hip and lumbar spine;
Time frame: at week 52 compared to baseline
osteoporosis-related genotyping.
Time frame: During the study conduct
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