Summary:
Providea Health Partners is enrolling adults in a clinical research study to assess the safety and efficacy of an investigational implantable device for the treatment of urinary urge incontinence.
You may qualify, if you:
- Have a diagnosis of Urinary Urge Incontinence (UUI) for at least 6 months.
- Have tried non-medication therapy such as pelvic floor training, biofeedback or behavorial modification without success or you are not a good candidate for such treatment.
- Failed to respond and/or are intolerant to at least 2 overactive bladder medications.
Qualified Participants May Receive:
Qualified participants may receive:
- Investigational device implant at no cost.
- All study-related medical care at no cost.
- The opportunity to help advance medical research.•Compensation for study-related time and travel.
- Other criteria will be evaluated to see if you may participate in this study.