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NCT00765258 · ClinicalTrials.gov registry record
Utility of CT Fluoroscopy Guidance During Percutaneous Sacroplasty With Quality of Life Assessment
A clinical trial, sponsored by Medical College of Wisconsin.
- Completed
- Registry status
- 14
- Enrollment target
NCT00765258: Completed study, sponsored by Medical College of Wisconsin.
NCT00765258 is a clinical trial that has completed, run by Medical College of Wisconsin. The registered enrollment target is 14 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00765258 has completed, sponsored by Medical College of Wisconsin.
- COMPLETED
- Registry status
- 14 participants
- Enrollment target
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.
Primary Outcome
The average pre-treatment VAS score was significantly improved after sacroplasty in patients with sacral insufficiency fractures.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 14 participants |
| Start Date | 2008-01 |
| Est. Completion | 2013-02 |
What the finished NCT00765258 record still lists
NCT00765258 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 14 participants, a relatively small participant target.
The record links to 0 conditions, and to 0 interventions.
NCT00765258 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00765258 about?
NCT00765258 is a clinical study titled "Utility of CT Fluoroscopy Guidance During Percutaneous Sacroplasty With Quality of Life Assessment". 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...
What is the current status of trial NCT00765258?
This trial is currently completed. The enrollment target is 14 participants. The study started on 2008-01. Estimated completion is 2013-02.
Who is sponsoring clinical trial NCT00765258?
This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.
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