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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04751422
Other study ID # 2020-1012
Secondary ID NCI-2021-0060720
Status Recruiting
Phase
First received
Last updated
Start date November 13, 2020
Est. completion date September 30, 2023

Study information

Verified date April 2023
Source M.D. Anderson Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study collects data on the use of radiofrequency ablation and cement augmentation for the treatment of cancer that has spread to the spine (metastases to the spine). Radiofrequency ablation with cement augmentation is a useful approach for the treatment of secondary metastasis to the spine. Information collected in this study may help doctors to learn the effectiveness of this therapy, and may help to evaluate optimal technique, appropriate patient selection, and management of complications.


Description:

PRIMARY OBJECTIVE: I. To evaluate the use of radiofrequency ablation and cement augmentation for the treatment of secondary metastases to the spine. OUTLINE: Patients' medical data is collected retrospectively.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date September 30, 2023
Est. primary completion date September 30, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients who underwent radiofrequency ablation with cement augmentation at the Department of Interventional Radiology at MD Anderson Cancer Center (MDACC) between 1/1/2017 and 9/26/2020 Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms

  • Metastatic Malignant Neoplasm in the Spine
  • Neoplasms

Intervention

Other:
Electronic Health Record Review
Medical data is collected

Locations

Country Name City State
United States M D Anderson Cancer Center Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
M.D. Anderson Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Technical success Results will be compared with data available from other published literature. Up to 3 years
Primary Clinical success Results will be compared with data available from other published literature. Up to 3 years
Primary Complication rates Results will be compared with data available from other published literature. Up to 3 years
See also
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Active, not recruiting NCT02364557 - Testing Whether Treating Breast Cancer Metastases With Surgery or High-Dose Radiation Improves Survival Phase 2/Phase 3
Completed NCT02713269 - Thermal Ablation and Spine Stereotactic Radiosurgery in Treating Patients With Spine Metastases at Risk for Compressing the Spinal Cord Phase 2