SBRT in the Management of Solid Spinal Metastases
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-99
SponsorUniversitaire Ziekenhuizen KU Leuven
About this trial
Documenting efficiency of SBRT in the management of epidural spinal metastases from solid tumors
Eligibility criteria
Qualifiers
Radiological diagnosis of spinal metastasis from solid tumor with epidural imminent or actual spinal cord compression, with or without neurological deficits. Patients will be scheduled for surgery + SBRT. If contra-indications preclude surgery and only SBRT is performed, patients will still be included.
Written informed consent to participate in the study must be obtained from the subject or proxy /legal representative
Males and females > 18 years
Disqualifiers
Any concomitant condition or disease which, in the opinion of the investigator, would affect the reliability of the collected data.
Patients that had previous radiotherapy on the index spinal level without the possibility for additional SBRT at that particular level.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Source ClinicalTrials.gov