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Clinical Trial Summary

The purpose of this study is to determine the duration of the treatment with alendronate in postmenopausal women with osteoporosis.


Clinical Trial Description

The duration of the treatment with alendronate is not well established. The investigators recruited 228 women with postmenopausal osteoporosis. They all received alendronate during the first 3 years of monitoring and were later on randomized to whether different regimens of intermittent treatment or to carry on 3 years more. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00936260
Study type Interventional
Source Ciudad Universitaria, Spain
Contact
Status Completed
Phase N/A
Start date January 1998
Completion date December 2004

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