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Clinical Trial Summary

This observational cohort study is being conducted to further characterize selected adverse events of interest among a patient population with osteoporosis who are prescribed bazedoxifene, raloxifene, or a bisphosphonate in usual clinical care outside of a randomized clinical trial setting. The study will compare the rates of the selected clinical events among the three treatment groups.


Clinical Trial Description

All women in the database meeting the inclusion criteria will be included in the study without any statistical sampling. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01416194
Study type Observational
Source Pfizer
Contact
Status Completed
Phase
Start date July 25, 2011
Completion date April 30, 2019

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