Actively Recruiting
Home Versus Office Removal of Percutaneous Nerve Evaluation (PNE) Lead
Led by The Cleveland Clinic · Updated on 2026-01-23
30
Participants Needed
1
Research Sites
186 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Home Versus Office Removal of Percutaneous Nerve Evaluation (PNE) Lead
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age greater than or equal to 18 years of age
- Patients undergoing sacral neuromodulation (SNM) for urinary urgency incontinence or urgency-frequency syndrome
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cleveland Clinic
Cleveland, Ohio, United States, 44195
Actively Recruiting
Research Team
C
Cecile A. Ferrando, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here