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Clinical Trials/NCT00765258
NCT00765258
Completed
Not Applicable

Utility of CT Fluoroscopy Guidance During Percutaneous Sacroplasty With Quality of Life Assessment

Medical College of Wisconsin1 site in 1 country14 target enrollmentJanuary 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sacro-iliac Insufficiency Fractures
Sponsor
Medical College of Wisconsin
Enrollment
14
Locations
1
Primary Endpoint
Reduction of pain and improved mobility in patients post percutaneous sacroplasty effectively assessed using the VAS pain scale and RMDQ both pre and post procedure.
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

To examine, through retrospective and prospective chart review, the difference in pain and mobility, pre and post treatment, as assessed by the patient's completion of the VAS pain scale and Roland Morris Disability Questionnaire (RMDQ).

CT fluoroscopy guidance during percutaneous sacroplasty is an effective treatment for sacro-iliac insufficiency fractures resulting in rapid reduction of pain and improved mobility in patients. This can be effectively assessed using the VAS pain scale and RMDQ both pre and post procedure.

Detailed Description

The purpose of the study is to report the use of CT fluoroscopy guidance during the performance of percutaneous sacroplasty. In addition, clinical results will be reported with the Roland Morris Disability Questionnaire(RMDQ)pre and post procedure, demonstrating the utility of the RMDQ in assessing improvement in patients pain, mobility and ability to perform activities of daily living.

Registry
clinicaltrials.gov
Start Date
January 2008
End Date
February 2013
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sean Tutton, MD

Principal Investigator

Medical College of Wisconsin

Eligibility Criteria

Inclusion Criteria

  • greater than 18 years of age and treated with or about to be treated with percutaneous CT fluoro-guided sacroplasty, regardless of gender or ethnicity.

Exclusion Criteria

  • less than 18 years old
  • pregnancy
  • inability to complete forms and surveys

Outcomes

Primary Outcomes

Reduction of pain and improved mobility in patients post percutaneous sacroplasty effectively assessed using the VAS pain scale and RMDQ both pre and post procedure.

Time Frame: 2008-2012

The average pre-treatment VAS score was significantly improved after sacroplasty in patients with sacral insufficiency fractures.

Study Sites (1)

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