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A Study To Assess The Quality Of Bone In Patients Taking Oral Ibandronate Versus Placebo

Osteoporosis Clinical Trial

Official title:
A One Year, Parallel, Placebo-controlled, Double-blind, Randomized Study to Assess the Effect of Monthly 150mg Oral Ibandronate Dosing Versus Placebo on Bone Quality and Strength at the Proximal Femur in Women With Osteoporosis

Clinical Trial Summary

The purpose of this study is to estimate the effect of oral Boniva (ibandronate sodium)taken once monthly versus placebo on bone quality and strength at the hip at one year.

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02948881
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 4
Start date August 2005
Completion date July 2007
View Details
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