Home Versus Office Removal of Percutaneous Nerve Evaluation (PNE) Lead

Completed · Not applicable

Conditions studied: Overactive Bladder

In brief

For women undergoing percutaneous nerve evaluation (PNE) for the treatment of overactive bladder the first step is the PNE interstim therapy trial. If the PNE works, patients may opt to have the interstim procedure. The purpose of this study is to see if patients who remove their PNE lead at home have the same satisfaction with the PNE trial as those women who have their lead removed in the office.

Key facts

Study ID

NCT05799313

Run by

The Cleveland Clinic

People needed

30

Starts

2023-06-07

Expected to finish

2026-07-22

Last updated by the study team

2026-07-23

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Age greater than or equal to 18 years of age
• Patients undergoing sacral neuromodulation (SNM) for urinary urgency incontinence or urgency-frequency syndrome

You may not qualify if…

• Inability to comprehend written and/or spoken English
• Inability to provide informed consent
• Patients undergoing SNM for other indications (e.g. urinary retention, fecal incontinence,)
• Previous SNM treatment
• No home support to assist with lead removal

Where it is running

• Cleveland Clinic — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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