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Metastatic Spinal Cord Compression (MSCC): Treatment Timing and Survival Rate

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National Taiwan University

Status

Unknown

Conditions

Neoplasm Metastasis
Spinal Cord Compression

Treatments

Other: Palliative Decompression

Study type

Observational

Funder types

Other

Identifiers

NCT02934594
201608007RIND

Details and patient eligibility

About

Patients with metastatic spinal cord compression (MSCC) are treated with different options according to the life expectancy. Survival and surgical outcome can be influenced by surgical timing in MSCC patients treated with palliative decompression.

Full description

MSCC patients who underwent palliative decompression after January 2012 in National Taiwan University Hospital (NTUH) were divided into the preoperative motor function intact group (Group A) and motor deficit group (Group B). The motor deficit group was subdivided into operation within 48 hours (Group B1), and after 48 hours (Group B2). All patients underwent palliative decompression and posterior stabilization. Investigators did wide laminectomy for tumor invading the vertebral body, and debulking surgery for tumor destructing the posterior column of the spine. Investigators retrospectively reviewed all patient records, including patient demographics, prognostic factors for survival (Kaplan-Meier survival analysis), neurological outcome (Frankel grade), primary tumor, complications, and relevance of Tomita and Tokuhashi scores.

Enrollment

500 estimated patients

Sex

All

Ages

21 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with metastatic spinal cord compression (MSCC) who underwent palliative decompression in National Taiwan University Hospital after January 1st, 2012.

Exclusion criteria

  • Patients with metastatic spinal cord compression (MSCC) who underwent palliative decompression before December 31st, 2011, or those who were not treated in National Taiwan University Hospital.

Trial design

500 participants in 3 patient groups

Group A
Description:
Motor function intact group: received palliative decompression
Treatment:
Other: Palliative Decompression
Group B1
Description:
motor deficit group: received palliative decompression within 48 hours after symptoms occured
Treatment:
Other: Palliative Decompression
Group B2
Description:
motor deficit group: received palliative decompression 48 hours after symptoms occured
Treatment:
Other: Palliative Decompression

Trial contacts and locations

0

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Central trial contact

Shu-Hua Yang, M.D., Ph.D.

Data sourced from clinicaltrials.gov

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