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A Study That Will Compare the Effect of Two Drugs on Participants With Low Bone Mass and a Recent Hip Fracture — MOVE  

Osteoporosis Clinical Trial

Official title:
Comparison of the Effects of Teriparatide With Those of Risedronate on Lumbar Spine BMD (Bone Mineral Density) in Men and Postmenopausal Women With Low Bone Mass and a Recent Pertrochanteric Hip Fracture

Clinical Trial Summary

This study will evaluate whether teriparatide is superior to the active comparator in the change from baseline of lumbar spine BMD (bone mineral density) in men and postmenopausal women with low bone mass and a recent pertrochanteric hip fracture.

Clinical Trial Description

The study has 3 periods: a screening phase, a double-blind, double-dummy treatment phase from the time of randomization to the 26 weeks visit, and an open-label treatment phase of approximately 12 month duration, where participants will continue treatment with the same study drug that they were randomized to. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00887354
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 4
Start date April 2009
Completion date August 2015
View Details
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