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The Kiva® System as a Vertebral Augmentation Treatment — KAST  

Spinal Fractures Clinical Trial

Official title:
The Kiva® System as a Vertebral Augmentation Treatment - A Safety and Effectiveness Trial

Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of the Kiva VCF Treatment system in comparison to balloon kyphoplasty for the treatment of osteoporotic vertebral compression fractures of the thoracic or lumbar spine.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01123512
Study type Interventional
Source Benvenue Medical, Inc.
Contact
Status Completed
Phase Phase 3
Start date July 2010
Completion date May 2013
View Details
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