Trials / Completed
CompletedNCT05884372
Efficacy and Safety of Combination Denosumab With Eldecalcitol for Postmenopausal Women With Osteoporosis.(ESCORT)
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Xi'an Honghui Hospital · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Primary objective: To compare the bone mineral density (BMD) change under the treatment of denosumab with eldecalcitol or native vitamin D in postmenopausal women with osteoporosis on bone mineral density. Secondary objective: To compare the efficacy of denosumab with eldecalcitol or native vitamin D treatment in postmenopausal women with osteoporosis on bone turnover markers, serum PTH, serum calcium, serum phosphorus, muscle mass, muscle strength, body balance ability, and quality of life.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Eldecalcitol | the same as arm descriptions. |
| DRUG | Native Vitamin D | the same as arm descriptions. |
| DRUG | Denosumab | the same as arm descriptions. |
| DRUG | Calcium | the same as arm descriptions. |
Timeline
- Start date
- 2023-08-24
- Primary completion
- 2025-07-16
- Completion
- 2025-07-16
- First posted
- 2023-06-01
- Last updated
- 2025-11-24
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT05884372. Inclusion in this directory is not an endorsement.