Outcomes of Pudendal InterStim
Status
Conditions
Details and patient eligibility
About
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).
Full description
InterStim is a bladder pacemaker device that has been in use for over 10 years for patients with voiding dysfunction. Although standard of care is to place the lead at the sacral nerve, in some patients a better response is obtained by placing the lead at the pudendal nerve.
Data will be collected from the subjects medical records and a questionnaire will be mailed one time to assess patients perception of improvement and treatment satisfaction after pudendal Interstim.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- All patients having had Interstim with a pudendal lead at Beaumont
Exclusion criteria
- None
Trial design
84 participants in 1 patient group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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