Trials / Unknown
UnknownNCT03006003
Osteoporosis Treatment in Post-menopausal Women
The Assessment of Osteoporosis Treatment in Post-menopausal Women
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 500 (estimated)
- Sponsor
- Taichung Veterans General Hospital · Academic / Other
- Sex
- Female
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
The study will be conducted to assess the depressive symptoms and related markers in the postmenopausal female after anti-osteoporosis treatment.
Detailed description
Fracture is one of the important complications in female. Osteoporosis should be treated in postmenopausal female due to high risk of fracture. Recently, there have been many classes of medications developed for preventing bone loss. Raloxifene, an oral form of anti-osteoporosis medication, has been reported to improved central nervous disorders. Therefore, this study is designed to assess the depressive symptoms and related markers in the postmenopausal female after anti-osteoporosis treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Raloxifene | Raloxifene tratment more than 4 weeks |
| DRUG | Alendronate | Alendronic acid 70mg with Colecalciferol 70mcg |
Timeline
- Start date
- 2017-01-01
- Primary completion
- 2021-12-01
- Completion
- 2021-12-01
- First posted
- 2016-12-30
- Last updated
- 2019-01-14
Locations
2 sites across 1 country: Taiwan
Source: ClinicalTrials.gov record NCT03006003. Inclusion in this directory is not an endorsement.