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Clinical Trial Summary

This study is a regulatory post-marketing surveillance in Japan, and it is a local prospective and observational study of patients who have received Julina for postmenopausal osteoporosis. The objective of this study is to assess safety and efficacy of using Julina in clinical practice. A total 100 patients will be recruited and followed 3 years since starting Julina administration.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01386281
Study type Observational
Source Bayer
Contact
Status Completed
Phase
Start date October 20, 2008
Completion date April 15, 2014

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