Percutaneous Nerve Evaluation With Fluoroscopy Versus Without

Completed · Not applicable

Conditions studied: Overactive Bladder, Urinary Incontinence, Fecal Incontinence

In brief

The investigators propose a randomized control trial comparing the rate of implantation of the InterStim device following Percutaneous Nerve Evaluation (PNE) performed with or without fluoroscopic guidance.

Key facts

Study ID

NCT02677753

Run by

University of Louisville

People needed

75

Starts

2016-04-01

Expected to finish

2019-04-01

Last updated by the study team

2020-06-09

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women age >18
• English speakers
• Patients with urinary urgency, frequency, or urge incontinence refractory to at least 1 other intervention who elect to undergo PNE

You may not qualify if…

• Patients in whom bilateral leads cannot be placed
• Pregnant women
• Prisoners
• Less than 18 years of age

Where it is running

• University of Louisville Physicians — Louisville, Kentucky, United States

Full record on ClinicalTrials.gov

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