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Clinical Trial Summary

This study is to evaluate and compare the effects of Alendronate and Risedronate to treat women with postmenopausal osteoporosis. The primary hypothesis for this study is that in postmenopausal women with osteoporosis, treatment with oral alendronate 70 mg once weekly will produce a mean percent increase from baseline in hip trochanter bone mineral density (BMD) at 12 and 24 months which is greater than that observed with oral risedronate 35 mg once weekly.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00092014
Study type Interventional
Source Organon and Co
Contact
Status Completed
Phase Phase 3
Start date September 1, 2002
Completion date April 1, 2004

See also
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