Cyberknife Radiosurgery and Quality of Life
Terminated
- Conditions
- Bone CancerCentral Nervous System Cancer
- Registration Number
- NCT01163539
- Lead Sponsor
- Stanford University
- Brief Summary
The purpose of this study is to look at pain control and QOL improvement after treatment with CK Radiosurgery for spinal metastases.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 15
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 40.
- Negative pregnancy test or clinically assessed as not pregnant.
- Ability to understand and the willingness to sign a written informed consent document.
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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.
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Stanford University School of Medicine
🇺🇸Stanford, California, United States