Potential Vertebroplasty Use in the Treatment of Vertebral Metastasis From Breast and Prostate Cancer

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2006 by McGill University Health Center.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
McGill University Health Center
ClinicalTrials.gov Identifier:
NCT00294151
First received: February 17, 2006
Last updated: July 12, 2007
Last verified: January 2006

February 17, 2006
July 12, 2007
September 2005
Not Provided
pain relief; score on pain questionnaire [ Time Frame: at baseline, 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after ]
pain relief; score on pain questionnaire at (baseline,) 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after.
Complete list of historical versions of study NCT00294151 on ClinicalTrials.gov Archive Site
  • quality of life; score on 2 quality of life questionnaires [ Time Frame: at baseline, 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after ]
  • pain medication [ Time Frame: listed at baseline, 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after ]
  • side effects [ Time Frame: listed at 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after ]
  • cost of medical care [ Time Frame: evaluated at baseline, 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after ]
  • survival [ Time Frame: recorded at 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after ]
  • new vertebral fractures [ Time Frame: recorded at 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after ]
  • quality of life; score on 2 quality of life questionnaires at (baseline,) 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after.
  • pain medication; listed at (baseline,) 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after.
  • side effects; listed at 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after.
  • cost of medical care; evaluated at (baseline,) 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after.
  • survival; recorded at 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after.
  • new vertebral fractures; recorded at 1 week, 2 weeks, 4 weeks, 3 months, 6 months, 1 year after.
Not Provided
Not Provided
 
Potential Vertebroplasty Use in the Treatment of Vertebral Metastasis From Breast and Prostate Cancer
Challenging the Paradigm in Pain Relief for Advanced Breast and Prostate Cancer Patients With Vertebral Metastasis: Vertebral Augmentation With Cement Plus Radiotherapy Versus Radiotherapy. A Randomized, Prospective, Double Blind Pilot Study

The study aims to evaluate if adding vertebroplasty to radiotherapy, in the treatment of spine metastasis from breast and prostate cancer, is preferable to radiotherapy alone. The investigators hypothesize that, by combining vertebral augmentation with cement and radiotherapy, they could achieve an enhancement in pain relief and level of activities, as well as a decrease in the side effects of multiple medications used for pain control.

Included patients presenting with spinal metastasis secondary to breast or prostate cancer are randomized to two groups, intervention and control. Both groups receive standard radiotherapy, which is currently the gold standard of care for such patients. The intervention group will also receive a vertebroplasty [single or multiple level(s)], while the control group will receive a simulated vertebroplasty, where local anesthesia and gentle hand manipulation will be used but the vertebra will not be accessed. The primary outcome is pain relief, though other factors such as quality of life and pain medications will also be evaluated.

There will be an interim analysis after half of the patients have been treated with a follow-up of 3 months. In the analysis, comparisons will be made between the two groups and each patient's individual progress will also be analyzed.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
  • Breast Cancer
  • Prostate Cancer
  • Vertebral Metastasis
  • Pain
Procedure: Vertebroplasty
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
30
Not Provided
Not Provided

Inclusion Criteria:

  • Between 35 and 75 years old
  • Biopsy-proven breast cancer (BC) or prostate cancer (PC)
  • Radiographic evidence of spine metastases from the BC or PC in the lumbar and/or mid-low thoracic spine
  • Microfractures or compression fractures up to 40% of the original height of the vertebral body in an MRI [magnetic resonance imaging] (reported by an independent radiologist)
  • Incidental back pain (Verbal Analog Scale > 5/10) felt to be related to those metastases

Exclusion Criteria:

  • Spinal cord compression
  • Massive rupture of the posterior wall of the vertebral body (according to blinded radiological report)
  • Coagulopathy (International Normalized Ratio [INR] > 1.5, platelets < 80,000)
  • Inability to communicate in English, French or Spanish
  • Previous radiotherapy to the spine in the area presently affected
  • Mental cognitive impairment
  • Vertebral metastasis without fracture in the MRI
Both
35 Years to 75 Years
No
Contact: Juan F Asenjo, MD 514-934-1934 ext 43261 jfasenjog@yahoo.com
Canada
 
NCT00294151
GEN#05-015
Not Provided
Not Provided
McGill University Health Center
Not Provided
Principal Investigator: Juan F Asenjo, MD Montreal General Hospital
McGill University Health Center
January 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP