This study seeks to examine the response of the bladder to different pudendal nerve stimulation frequencies, by studying patients who have been previously-implanted with pudendal nerve neurostimulators.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Previously received an implanted neurostimulator at the pudendal nerve
* Adult (18 or older), capable of providing own informed consent and communicating clearly with the research team
* Capable of speaking, reading, and understanding English, as all study questionnaires are standardized assessments only available in English.
* Capable of attending the experimental session
Exclusion Criteria:
* Pregnant or planning to become pregnant during study. If a woman of child- bearing potential wishes to participate in this study, they will be pre-screened with a test to detect pregnancy
* Currently has a urinary tract infection (UTI)
* Currently has or tested positive in the last 14 days for COVID-19, or is symptomatic for COVID-19
* Unwilling to allow de-identified data to be stored for future use or shared with other researchers
What they're measuring
1
Evoked Bladder Contractions of at Least 20 Centimeters of Water (cmH2O) During Cystometrogram
Timeframe: Visit 1, approximately 1 week after consent