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Study identifier: NCT07135817 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Preoperative Stereotactic Radiotherapy for Treatment of Spinal Metastases

Condition: Spinal Metastases · Solid Tumor Cancer  ·  Sponsor: University Medical Center Goettingen

PhaseNA
Planned participants20
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this interventional clinical trial is to evaluate the efficacy and safety of preoperative hypofractionated Stereotactic Body Radiotherapy (SBRT) in the treatment of patients undergoing surgery for spinal metastases. The main questions this study aims to answer are: * Does preoperative SBRT result in local tumor control at the involved spinal segments as assessed by MRI/CT scan at 3 and 6 months postoperatively? * What are the postoperative outcomes in terms of pain intensity, functional status and quality of life? Participants will receive hypofractionated SBRT to spinal metastases shortly before surgical intervention. Participants will undergo preoperative and follow-up assessments, including: * MRI and CT scans before and after surgery and at 3 and 6 months after surgery to measure tumor size * Pain questionnaires where patients rate their current pain, worst pain, and average pain in the last 24 hours on a scale from 0 (no pain) to 10 (worst pain imaginable) * A short questionnaire (Karnofsky Performance Status) to assess the patient's general ability to carry out daily activities * Several patient questionnaires to evaluate back pain, physical limitations, and overall quality of life (Oswestry Disability Index, EORTC QLQ-C30, and EORTC QLQ-BM22)

This description comes directly from the study's public registry record.

Talk to the study team

Carla Marie Zwerenz, Dr. med.  ·  +49 551 39 64501  ·  carlamarie.zwerenz@med.uni-goettingen.de

Always discuss trial participation with your own doctor first.

Locations (1)

University Medical Center GoettingenGöttingen, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT07135817