Denosumab Sequential Therapy (DST)
Osteoporosis
About this trial
This is an interventional treatment trial for Osteoporosis focused on measuring Osteoporosis, Denosumab, Zoledronate, Bone mineral density
Eligibility Criteria
Inclusion Criteria:
- Postmenopausal women
- Men >50-year-old
- After Denosumab treatment ≥ 2 years due to osteoporosis
Exclusion Criteria:
- secondary osteoporosis
- metabolic bone disease
- cancer history
- continuous steroid therapy
- hormone replacement therapy
- ever used any other kind of anti-resorptive treatment
6.estimated Glomerular filtration rate< 35 mL/min 7.allergy to Zoledronic acid 8.hypocalcaemia 9.any contraindications to use Zoledronic acid
Sites / Locations
- Department of Orthopedics, National Taiwan University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Experimental
Experimental
Continuous Denosumab
Zoledronic acid to Denosumab
Continuous Zoledronic acid
Zoledronic acid to observation
Continuous anti-resorptive therapy by Denosumab for 2 years
treat with Zoledronic acid for one year and then shift to Denosumab for another one year
Continuous anti-resorptive therapy by Zoledronic acid for 2 years
treat with Zoledronic acid for one year and then close follow up by bone turn over marker. resume another dose of Zoledronic acid if elevated CTX level above normal range