Outcomes of Pudendal InterStim
Completed
Conditions studied: Voiding Dysfunction
In brief
The purpose of this study is to determine how many patients who have failed treatment with a sacral lead can achieve good results with a pudendal, patients satisfaction with the results of each lead, complication rates after pudendal lead placement, and how many patients have required reprogramming of their device with EMG testing( a more costly procedure).
Key facts
- Study ID
- NCT00719589
- Run by
- Corewell Health East
- People needed
- 84
- Starts
- 2008-07-01
- Expected to finish
- 2010-01-01
- Last updated by the study team
- 2010-03-24
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All patients having had Interstim with a pudendal lead at Beaumont
You may not qualify if…
- None
Where it is running
- William Beaumont Hospital-Royal Oak — Royal Oak, Michigan, United States
Full record on ClinicalTrials.gov
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