Trials / Unknown
UnknownNCT03702140
Examination How the Administration Period of Teriparatide Affects Bone Metabolism and Bone Mineral Density Prior to Denosumab Therapy
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 90 (estimated)
- Sponsor
- Shinshu University · Academic / Other
- Sex
- All
- Age
- 20 Years – 120 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to examine the efficacy and adverse events in the following 3 groups in osteoporosis patients: 1. The administration period of teriparatide is less than 6 months and thereafter, denosumab for 24 months. 2. The administration period of teriparatide is from 6 to 12 months and thereafter, denosumab for 24 months. 3. The administration period of teriparatide is more than 12 months and thereafter, denosumab for 24 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | "Teriparatide", "Forteo® or Teribon" | To examine the effects of terimaratide less than 6 months in osteoporosis |
Timeline
- Start date
- 2018-10-09
- Primary completion
- 2023-10-08
- Completion
- 2025-10-08
- First posted
- 2018-10-10
- Last updated
- 2021-09-21
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT03702140. Inclusion in this directory is not an endorsement.