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Clinical Trial Summary

Patients with vertebral compression fracture will be treated cement injection into the spine and monitored using standard evaluations.


Clinical Trial Description

Patients with vertebral compression fracture will be diagnosed and treated with balloon kyphoplasty. Pain and functional status will be assessed at baseline, 1-, 12-, and 24-months post-operatively using VAS pain scale, Oswestry Disability Index, and SF-36. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00166374
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase N/A
Completion date June 2007

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