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Effects of Teriparatide or Denosumab on Bone in Postmenopausal Women With Osteoporosis

Osteoporosis Clinical Trial

Official title:
Anabolism Versus Antiresorption: A Quadruple Labeling Histomorphometry Study to Compare the Mechanism of Action of Teriparatide and Denosumab in Postmenopausal Women With Osteoporosis

Clinical Trial Summary

The purpose of this study is to determine how teriparatide or denosumab affects the bone of postmenopausal women with osteoporosis after 3 months of treatment, as determined by a bone biopsy sample taken from the iliac crest (upper part of the pelvis).

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01753856
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 4
Start date January 2013
Completion date June 2014
View Details
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