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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01163539
Other study ID # SPN0002
Secondary ID SU-07092010-6499
Status Terminated
Phase N/A
First received July 14, 2010
Last updated June 29, 2016
Start date July 2010
Est. completion date June 2012

Study information

Verified date June 2016
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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


Recruitment information / eligibility

Status Terminated
Enrollment 15
Est. completion date June 2012
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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.

Study Design

Observational Model: Ecologic or Community, Time Perspective: Prospective


Locations

Country Name City State
United States Stanford University School of Medicine Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

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