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SBRT in the Management of Solid Spinal Metastases

Documenting efficiency of SBRT in the management of epidural spinal metastases from solid tumors

Condition(s)Extradural Tumor, Spinal Metastases
StatusRecruiting
Study typeObservational
SummaryDocumenting efficiency of SBRT in the management of epidural spinal metastases from solid tumors
Who can participateInclusion Criteria: * 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 Exclusion Criteria: * 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.
Ages18 Years to 99 Years
SexAll
Lead sponsorUniversitaire Ziekenhuizen KU Leuven
LocationsLeuven, Vlaams Brabant, Belgium
Start date2021-05-18
NCT IDNCT04863612
Official listinghttps://clinicaltrials.gov/study/NCT04863612

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