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Delineation of Target Volume of Stereotactic Radiotherapy for Spinal Tumors (ST-SBRT)

P

Peking University

Status

Enrolling

Conditions

Spinal Tumor

Treatments

Radiation: Target volume delineation

Study type

Observational

Funder types

Other

Identifiers

NCT06587022
ST-SBRT

Details and patient eligibility

About

The purpose of this study was to compare efficacy and side effects of two target delineation methods for stereotactic radiotherapy of metastatic spinal tumors.

Full description

The purpose of this study was to compare efficacy and side effects of two target delineation methods for stereotactic radiotherapy of metastatic spinal tumors. This is a bidirectional cohort study planned to enroll approximately 500 patients with metastatic spinal tumors. Patients are divided into two groups according to the target delineation method. Group 1:The target bolume only includes local tumor. Group 2:The target bolume includes local tumor and adjacent vertebral area.

Enrollment

500 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with spinal metastases or primary tumors receiving stereotactic radiotherapy;
  • Patients with sufficent pre-treatment imaging data
  • Patients who can cooperate with imaging review and follow-up after radiotherapy.

Exclusion criteria

  • Patients with an expected survival of less than 3 months;
  • Patients with second-course radiotherapy;
  • Patients with physical conditions that cannot tolerate stereotactic radiotherapy;
  • Patients with extensive spinal metastasis and no local therapeutic value

Trial design

500 participants in 2 patient groups

group 1
Description:
Group 1(small target delineation):The target bolume only includes local tumor.
Treatment:
Radiation: Target volume delineation
group 2
Description:
Group 2(small target delineation):The target bolume includes local tumor and adjacent vertebral area.
Treatment:
Radiation: Target volume delineation

Trial contacts and locations

1

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Central trial contact

Yuxia Wang; Hongqing Zhuang, Doctor

Data sourced from clinicaltrials.gov

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