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Application of Spinal Bracket in Palliative Surgery for Spinal Metastatic Tumors with Combined Neurological Symptoms

Application of Spinal Bracket in Palliative Surgery for Spinal Metastatic Tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102871
Enrollment
Unknown
Registered
2025-05-21
Start date
2025-05-31
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal metastatic tumor

Interventions

3D-printed barriers group:3D-printed barrier
bone cement group:bone cement

Sponsors

Xi'an Jiaotong University Second Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-80 years; 2. Pathologically diagnosed with spinal metastasis; 3. Imaging shows spinal cord compression and vertebral mass, with symptoms consistent with imaging findings; 4. No concomitant conditions affecting spinal cord function, such as traumatic fractures or severe lumbar degenerative diseases; 5. Expected survival time of more than 6 months; 6. General condition allows for tolerance of surgery; 7. Tomita score between 4-7, candidate for marginal or intralesional tumor resection, palliative decompression, and stabilization surgery; 8. SINS score > 7, requiring surgery for stabilization; 9. Willing to participate and signs the informed consent form;

Exclusion criteria

Exclusion criteria: 1. History of spinal or spinal cord injury or previous spinal surgery; 2. Patients with primary spinal tumors or solitary bone metastasis requiring radical surgery; 3. Patients undergoing conservative treatment; 4. Combined with brain metastases; 5. Combined with cranial trauma, central nervous system diseases, etc; 6. Death within 6 months post-surgery; 7. Frankel classification Grade A; 8. Patients in poor general condition who cannot tolerate surgery; 9. Patients unable to cooperate with completing the assessment;

Design outcomes

Primary

MeasureTime frame
Time to tumor recurrence causing spinal cord compression;Surgical safety assessment (bleeding volume);Postoperative functional evaluation (VAS);Evaluation of the postoperative position of the spacer and cement, and the extent of bone destruction;Postoperative functional evaluation (JOA);Evaluation of postoperative bone tumor progression and spinal canal volume;Evaluation of postoperative bone tumor progression and extent of bone destruction;

Secondary

MeasureTime frame
Surgical safety assessment (surgical duration);Surgical safety assessment (number of fluoroscopy);

Countries

China

Contacts

Public ContactZhao Bo

Xi'an Jiaotong University Second Affiliated Hospital

13892846285@163.com+86 13892846285

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026