Actively Recruiting

Age: 18Years +
All Genders
NCT07479199

Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of Painful Thoracic and Lumbar Spine Tumors

Led by UNC Lineberger Comprehensive Cancer Center · Updated on 2026-04-23

70

Participants Needed

1

Research Sites

258 weeks

Total Duration

On this page

Sponsors

U

UNC Lineberger Comprehensive Cancer Center

Lead Sponsor

M

Medtronic

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study looks at how well a combination of treatments helps reduce pain in people with tumors in the middle and lower back (thoracic and lumbar spine). All participants receive the same treatment, which includes a procedure to stabilize the spine (kyphoplasty), radiofrequency ablation will be with the Osteocool system and radiation therapy. The goal is to see how effective this combined approach is at relieving pain. The purpose of this study is to find out whether combining these three treatments provides better pain relief for patients with thoracic and lumbar spine tumors. This study is for adults who have cancer that has spread to the thoracic or lumbar spine and who report moderate to severe back pain (a pain score of 5 or higher on a 0-10 pain scale).

CONDITIONS

Official Title

Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of Painful Thoracic and Lumbar Spine Tumors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Written informed consent and HIPAA authorization provided
  • Able and willing to follow study procedures
  • Age 18 years or older at consent
  • Life expectancy longer than 1 month and suitable for treatment
  • Metastatic tumor in thoracic or lumbar spine, with lytic or mixed lytic/blastic tumor type
  • Back pain score of 5 or higher on a visual analog scale
Not Eligible

You will not qualify if you...

  • Active infection needing systemic therapy
  • Pregnant or breastfeeding
  • Currently taking Avastin or blood thinners that cannot be stopped
  • Enrolled in another cancer clinical trial

AI-Screening

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Trial Site Locations

Total: 1 location

1

UNC Hospitals

Chapel Hill, North Carolina, United States, 27599

Actively Recruiting

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Research Team

M

Markeela Lipscomb

CONTACT

D

Desma Jones

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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