Percutaneous Nerve Evaluation Trial Time
Recruiting
N/A
Interventional Study
Urge Incontinence
Urgency-frequency Syndrome
Overactive Bladder
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 193 (estimated)
- Sponsor
- University of Chicago · Other
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About This Trial
Sacral neuromodulation (SNM) was approved by the Food and Drug Administration (FDA) for the treatment of urgency incontinence (UUI) in 1998. One of two trial phase techniques are utilized prior to placement of the implantable pulse generator (IPG) to predict a patient's success with the device: a percutaneous nerve evaluation (PNE) or a stage implantation. Patients who experience a \> 50% improvem…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Non-pregnant women \>/=18 years old undergoing sacral neuromodulation (SNM) treatment for urgency urinary incontinence (UUI) or urgency-frequency (UF) who have elected to undergo testing phase with a PNE
* \>/=5 UUI episodes on a 3-day bladder diary with urge incontinence repr…
Contacts