RECRUITINGPhase 2INTERVENTIONAL
Examination of Efficacy and Safety of Other Anti-Resorption Drugs After 2-year-Denosumab Therapy in Japanese Osteoporosis Patients
Examination of Efficacy and Safety of SERM or Bisphosphonates After 2-year-Denosumab Therapy in Japanese Osteoporosis Patients
About This Trial
The aim of this study is to examine the efficacy and adverse events in the following 3 groups in Japanese osteoporosis patients after 2-year-denosumab therapy: SERM and eldecalcitol treatment for 24 months Bisphosphonates and eldecalcitol treatment for 24 months Eldecalcitol treatment for 24 months
Who May Be Eligible (Plain English)
Who May Qualify:
- osteoporosis patients
Who Should NOT Join This Trial:
- not osteoporosis patients who are allergic to the drugs, refused to do this research, or who are pregnant
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* osteoporosis patients
Exclusion Criteria:
* not osteoporosis patients who are allergic to the drugs, refused to do this research, or who are pregnant
Treatments Being Tested
DRUG
SERM "Viviant®Tablet 20mg" and ELD "Edirol®Tablet 0.75ug"
To examine the effects of SERM and ELD in osteoporosis patients
DRUG
Bisphosphonates and ELD "Edirol®Tablet 0.75ug"
To examine the effects of BP and ELD in osteoporosis patients
DRUG
ELD "Edirol®Tablet 0.75ug"
To examine the effects of ELD in osteoporosis patients
Locations (1)
Yukio Nakamura
Matsumoto, Nagano, Japan