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Julina Post-marketing Surveillance for Postmenopausal Osteoporosis in Japan

Osteoporosis, Postmenopausal Clinical Trial

Official title:
Drug Use Investigation of Julina Tablets 0.5 mg (Postmenopausal Osteoporosis)

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

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01397955
Study type Observational
Source Bayer
Contact
Status Completed
Phase N/A
Start date January 2009
Completion date April 2014
View Details
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