Trials / Completed
CompletedNCT00765258
Utility of CT Fluoroscopy Guidance During Percutaneous Sacroplasty With Quality of Life Assessment
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 14 (actual)
- Sponsor
- Medical College of Wisconsin · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Timeline
- Start date
- 2008-01-01
- Primary completion
- 2012-05-01
- Completion
- 2013-02-01
- First posted
- 2008-10-02
- Last updated
- 2013-08-21
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00765258. Inclusion in this directory is not an endorsement.