Utility of CT Fluoroscopy Guidance During Percutaneous Sacroplasty With Quality of Life Assessment
Completed
Conditions studied: Sacro-iliac Insufficiency Fractures
In brief
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.
Key facts
- Study ID
- NCT00765258
- Run by
- Medical College of Wisconsin
- People needed
- 14
- Starts
- 2008-01-01
- Expected to finish
- 2013-02-01
- Last updated by the study team
- 2013-08-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- less than 18 years old
- pregnancy
- inability to complete forms and surveys
Where it is running
- Medical College of Wisconsin / Froedtert Hospital — Milwaukee, Wisconsin, United States
Full record on ClinicalTrials.gov
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