Identifying Stress Urinary Incontinence in Women With Pelvic Organ Prolapse
Stress Urinary Incontinence, Pelvic Organ Prolapse
About this trial
This is an interventional screening trial for Stress Urinary Incontinence focused on measuring Urodynamics, Pyridium pad test, Cough stress test, Pelvic organ prolapse
Eligibility Criteria
Inclusion Criteria:
- 18 y/o or greater
- Able to consent
- Stage 2 or greater prolapse
- With or without complaint of stress urinary incontinence
Exclusion Criteria:
- Desire non-surgical management
- Prior surgery for prolapse or incontinence
- Treated medically for incontinence in the past 4 weeks
- Current Infection
- Known neurologic condition
- Stage 3 or greater chronic kidney disease
Sites / Locations
- Cleveland Clinic Florida
Arms of the Study
Arm 1
Other
Urodynamics, pyridium pad & cough stress
The Pelvic Floor Bother Questionnaire, a questionnaire standardized by Cleveland Clinic Florida, the Urogenital Distress Inventory (UDI-6), and the numerical analog scale are to be administered prior to and 6 weeks after the surgical intervention. (14, 15) Prior to surgery, patients will be scheduled for a UDS performed by a qualified nurse practitioner or physician and will be given instructions in verbal and written form to undergo a 24 H pyridium pad test at least 72 hours before the UDS. Patients will be given pyridium TID and report if orange stain is noted on their pad in this period of time. A supine and a standing cough stress test will also be performed.