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Clinical Trials/NCT01163539
NCT01163539TerminatedNot Applicable

Cyberknife Radiosurgery and Quality of Life

Stanford University1 site in 1 country15 target enrollmentStarted: July 2010Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
15
Locations
1
Study OverviewStudy DesignEligibility CriteriaInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The purpose of this study is to look at pain control and QOL improvement after treatment with CK Radiosurgery for spinal metastases.

Study Design

Study Type
Observational
Observational Model
Ecologic Or Community
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients with a spinal metastasis who will be treated with Cyberknife radiosurgery.
  • •There are no age or gender restrictions.
  • •There are no life expectancy restrictions.
  • •Karnofsky Performance Status greater than
  • •Negative pregnancy test or clinically assessed as not pregnant.
  • •Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria

  • •Patients with benign tumors will not be included (neurofibromas, schwannomas, etc.)
  • •Other investigational medications or treatments will be noted, but will not preclude inclusion.
  • •Pregnant or nursing patients will be not be included in the study due to radiation exposure.

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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Cyberknife Radiosurgery and Quality of Life | Clinical Trial