The purpose of this multicenter, placebo-controlled, randomized clinical trial is to evaluate the safety and tolerability of 10 mg oral alendronate, administered with or without a 1000 mg elemental calcium supplement daily, compared to the 1000 mg elemental calcium supplement in the treatment of postmenopausal women with osteoporosis by assessing spine and hip bone mineral density at baseline and at 3, 6, 12, and 24 months of treatment.

Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
24
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02215
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