Approximately 20 women who meet the inclusion criteria will be enrolled in this triple-blind, randomized, multi-center, two-year study to compare the efficacy of daily oral alendronate vs. intranasal calcitonin vs. placebo in increasing lumbar spine bone density in ambulatory postmenopausal women with low bone denisty. Alendronate will be triple-blinded and calcitonin will be administered open-label.

Project Start
1999-12-01
Project End
2001-02-28
Budget Start
Budget End
Support Year
39
Fiscal Year
2000
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
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