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…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.