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Prospective Study Determining the Pain Response, Functional Interference and Quality of Life in Patients Undergoing Radiofrequency Ablation Assisted Vertebroplasty/ Cementoplasty (RFA)

S

Sunnybrook Health Sciences Centre

Status

Completed

Conditions

Quality of Life
Neoplasms
Cementoplasty

Treatments

Procedure: RFA Vertebroplasty

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Bone metastases are a cause of significant morbidity in cancer patients. In patients who die from breast, prostate, and lung cancer, autopsy studies have shown that up to 85% have evidence of bone metastases at the time of death (1). These metastases frequently give rise to complications that reduce patients' quality of life. These include: pain, fractures, and decreased mobility, ultimately reducing performance status.

Radiofrequency ablation therapy with cementoplasty/vertebroplasty for painful bone metastases has been shown to be feasible, efficacious, and safe. However, patient reported outcomes have yet to be determined.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Histologically or cytologically proven malignancy.
  2. Patients aged 18 and above.
  3. Advanced cancer with bone metastasis(es) to the spine and/or pelvis
  4. Symptomatic with axial pain from spinal lesions and at risk for pathological fracture, or, pathological fracture without spinal cord compromise
  5. Karnofsky Performance Status (KPS) greater than or equal to 40 at the time of baseline evaluation.
  6. Is planned to receive RFA and/or cementoplasty with treatment to all sites being followed for study.
  7. Is able to provide worst pain score at bony metastatic site(s).
  8. Patient is able and willing to fill out daily diary.
  9. Patients must be able to provide informed consent prior to being enrolled to the study.

Exclusion criteria

  1. Progressive neurological compromise
  2. Pathological fracture of vertebrae with significant cortical involvement or spinal canal compromise
  3. Central nervous system metastases
  4. Inability to record pain score, complete diary and communicate this to study personnel.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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