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Safety and Efficacy Study of Bugusan (BGS)to Treat Osteoporosis.

Osteoporosis Clinical Trial

Official title:
A Randomized, Double Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Effects on Biomarkers and Safety of Bugusan (BGS) in Postmenopausal Patients With Osteoporosis.

Clinical Trial Summary

The objective is to evaluate the effects on biomarkers and safety of BGS in postmenopausal patients with osteoporosis.

Clinical Trial Description

The objective is to evaluate the effects on biomarkers and safety of BGS in postmenopausal patients with osteoporosis by a study of Randomized, Double Blind, Placebo-Controlled, Parallel Group. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00202956
Study type Interventional
Source Taichung Veterans General Hospital
Contact Huey-Herng Sheu
Phone 8860402359-2525
Email whhsheu@vghtc.gov.tw
Status Recruiting
Phase Phase 2
Start date June 2004
Completion date May 2005
View Details
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