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Clinical Trial Summary

This study was conducted among women who had previously received alendronate for 3 to 6 years during the Fracture Intervention Trial (FIT). Participants in the FLEX study were randomly assigned to receive alendronate (either 5 or 10 mg/day) or matching placebo during the next 5 years, in order to evaluate the effects of continuing or discontinuing alendronate treatment on bone mineral density and biochemical markers of bone turnover.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00398931
Study type Interventional
Source Organon and Co
Contact
Status Completed
Phase Phase 3
Start date February 1998
Completion date October 2003

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