CPT Testing for Sacral Neuromodulation Outcomes
Completed · Not applicable
Conditions studied: Incontinence
In brief
This is a prospective study. Subjects will be recruited from the urology practices of Dr. Ken Peters and Dr. Ananias Diokno at William Beaumont Hospital. Subjects will be referred to the study by the clinician recommending Sacral NeuroModulation therapy (SNM). This pilot study is to explore the effect of SNM on sensory pathways by measuring CPT values pre and post SNM treatment.
Key facts
- Study ID
- NCT00617786
- Run by
- Corewell Health East
- People needed
- 13
- Starts
- 2008-10-01
- Expected to finish
- 2010-07-01
- Last updated by the study team
- 2011-11-23
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Established diagnosed overactive bladder
- Scheduled to receive SMN therapy by Dr. Peters or Dr. Diokno
- Women at least 18 years of age
- Capable of giving informed consent
- Capable and willing to follow all study related procedures (e.g. bladder and urethral catheterization, answering questions during CPT testing, complete questionnaires regarding pertinent medical history).
You may not qualify if…
- Current Urinary tract infection
- Currently participating or have participated within the past 30 days in any clinical investigation involving or impacting urinary or renal function.
- Pregnancy or intending to become pregnant during the study
- Cannot independently comprehend and complete relevant medical history questionnaires.
- The subject is deemed unsuitable for enrollment in this study by the investigators based on their history.
- Men are excluded
- TENS, PTNS or acupuncture therapy currently being used for symptoms
Where it is running
- William Beaumont Hospital — Royal Oak, Michigan, United States
Full record on ClinicalTrials.gov
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