Tuen Mun Hospital
Hong Kong, China
NCT Number: NCT01465568
The purpose of this study is to study the efficacy of denosumab, a new drug, in the treatment of osteoporosis in patients using bisphosphonates.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
Hong Kong, China
There are no data on the use of denosumab in steroid induced osteoporosis. Postmenopausal women with chronic use of Glucocorticoid (GCs) are at high-risk of osteoporotic fractures. Despite bisphosphonate treatment, a certain proportion of high-risk patients using chronic GCs either do not achieve a satisfactory gain in bone mineral density (BMD) or develop new fragility fractures. Thus, more potent osteoporosis treatment is necessary for this subgroup of patients. This prompts the current study which aims to examine the efficacy of denosumab in current users of oral bisphosphonates for Glucocorticoid-induced Osteoporosis (GIOP).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
60mg subcutaneous injection 6 monthly for 2 doses
Other names: Prolia
continue present bisphosphonate treatment
Other names: continuation of bisphosphonates in their usual dosages
Time frame: baseline, 6 months and 12 months
Time frame: baseline, 6 months and 12 months
Time frame: baseline, 6 months and 12 months
Time frame: 12 months
Time frame: 12 months
Tuen Mun Hospital
Other Gov
Denosumab in Current Users of Bisphosphonates for Glucocorticoid-induced Osteoporosis: a Randomized Controlled Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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