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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

TypeNameDescription
DRUGRaloxifeneRaloxifene tratment more than 4 weeks
DRUGAlendronateAlendronic 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.