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Safety and Effectiveness of Soy Phytoestrogens to Prevent Bone Loss — OPUS  

Osteoporosis Clinical Trial

Official title:
Safety, Efficacy, and Optimal Dosage of Soy Isoflavones to Prevent Osteoporosis

Clinical Trial Summary

The purpose of this study is to determine whether soy isoflavone supplementation is safe and effective to prevent bone loss in postmenopausal women.

Clinical Trial Description

Over-the-counter soy isoflavone supplement usage is becoming common among postmenopausal women. However, there is no documented scientific evidence of its long-term safety and efficacy in preventing osteoporosis. Our primary goal is to determine the safety, efficacy, and optimal dosage of isoflavone supplementation to reduce bone loss in postmenopausal women. The multi-state, multi-institutional design ensures that the study results are representative of postmenopausal women in the U.S. population. Confirming the skeletal benefits of soy isoflavones could translate into reduced healthcare costs related to osteoporosis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00665860
Study type Interventional
Source Baylor College of Medicine
Contact
Status Completed
Phase N/A
Start date April 2001
Completion date June 2006
View Details
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