Stereotactic Body Radiotherapy for Spine Tumors

Status Completed

Clinical Trial Summary

This study will evaluate the local control rate as well as acute and late toxicity rates of stereotactic body radiotherapy (SBRT) for the treatment of spine metastases and benign spine tumors.

Clinical Trial Description

This study is a single site, non-randomized, prospective, phase IV trial. Patients are composed of 2 groups:Spine Metastases OR Benign Spine Tumors. Data collected will include patient demographics, pathology data, tumor stage, SBRT dose fractionation scheme, dose received by adjacent critical normal tissues, tumor recurrence data, and acute and late toxicities.

Follow up data will be collected during the patient's standard office visits. The anticipated duration of this study is 5 years ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01347307
Study type	Interventional
Source	Mercy Research
Contact
Status	Completed
Phase	N/A
Start date	September 2008
Completion date	September 2017

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