The purpose of this clinical trial is to investigate a new medical device treatment for Overactive Bladder (OAB) in women.
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All device- and procedure-related adverse events will be collected and tabulated
Timeframe: Approximately 11 days in total
Urinary frequency
Timeframe: Approximately 11 days in total
Urinary urgency
Timeframe: Approximately 11 days in total
Urge urinary incontinence (UUI)
Timeframe: Approximately 11 days in total
OAB-q - Short Form
Timeframe: Approximately 11 days in total
OAB Symptom Score
Timeframe: Approximately 11 days in total
Urogenital Distress Inventory - Short Form
Timeframe: Approximately 11 days in total
Incontinence Impact Questionnaire - Short Form
Timeframe: Approximately 11 days in total