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

NCT00765258 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 14

Last updated 2013-08-21

No results posted yet for this study

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.

Conditions

  • Sacro-iliac Insufficiency Fractures

Sponsors & Collaborators

  • Winthrop University Hospital

    collaborator OTHER

  • Medical College of Wisconsin

    lead OTHER

Principal Investigators

  • Sean M Tutton, MD · Medical College of Wisconsin

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2012-05-31
Completion
2013-02-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00765258 on ClinicalTrials.gov