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Clinical Trial Summary

The purpose of this study is to determine pain control rate (Percentage of patients in each arm that achieve pain control) at the treated site(s) at 1 month, 2-4 months and 5-6 months post-treatment.


Clinical Trial Description

Eligible Vertebral Metastatic Lesion/s-> randomized-> SRT versus SRT+ VAP Stereotactic Radiation Therapy(SRT): 16 Gy X 1 Evaluation: prior to treatment; 1 month, 2-4 months, 5-6 months and 1 year post-treatment ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01527292
Study type Interventional
Source University of Louisville
Contact
Status Terminated
Phase N/A
Start date February 2012
Completion date September 2, 2015

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