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The Study of the Early Administration of Alendronate on Prevention of Bone Loss After Hip Fracture.

Osteoporosis Clinical Trial

Official title:
A Six Month Double-Blind, Placebo-Controlled Trial Followed by Six Month Open-Label Study of the Early Administration of Alendronate on Prevention of Bone Loss After Hip Fracture.

Clinical Trial Summary

To determine whether administration of Alendronate early is more effective than late in the prevention of osteoporosis following a hip fracture

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00346190
Study type Interventional
Source McGill University Health Center
Contact Richard Kremer, MD PhD
Phone 514-934-1934
Status Recruiting
Phase Phase 3
Start date January 2003
Completion date April 2007
View Details
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