Cyberknife Radiosurgery and Quality of Life

Status

Terminated

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01163539

Enrollment

Registered

2010-07-15

Start date

2010-07-31

Completion date

2012-06-30

Last updated

2016-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Cancer, Central Nervous System Cancer

Brief summary

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

Interventions

None listed

Study design

Observational model

ECOLOGIC_OR_COMMUNITY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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.

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.

Countries

United States

Outcome results