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Completed Not applicable Interventional Results available

Safety and Effectiveness of a Non-invasive Neuromodulation Device on Urgency Urinary Incontinence in Overactive Bladder

ClinicalTrials.gov ID: NCT01369485

Public ClinicalTrials.gov record NCT01369485. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:50 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multi-center, Prospective, Randomized, Double-blind, Sham-controlled Clinical Study to Evaluate Safety and Effectiveness of a Transcutaneous, High-frequency, Amplitude-modulated, Non-invasive Neuromodulation Device on Urgency Urinary Incontinence in Subjects With Overactive Bladder (OAB)

Study identification

NCT ID
NCT01369485
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Ethicon Endo-Surgery
Industry
Enrollment
163 participants

Conditions and interventions

Interventions

  • (VERV™ System) Device
  • Sham version of (VERV™ System) Device

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2011
Primary completion
Dec 31, 2012
Completion
Nov 30, 2013
Last update posted
Sep 10, 2014

2011 – 2013

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Arizona Urologic Specialists Tucson Arizona 85712-5803
Tri Valley Urology Medical Group Murrieta California 92562
GW Medical Faculty Associates Washington D.C. District of Columbia 20037
Specialists in Urology Naples Florida 34102
Urology Center of Florida Pompano Beach Florida 33060
Women's Health Institute of Illlinois, Ltd Oak Lawn Illinois 60453
1st Urology, PSC dba Metropolitan Urology Jeffersonville Indiana 47130
William Beaumont Hospital Royal Oak Michigan 48073
University Urology Associates New York New York 10016
McKay Urology Charlotte North Carolina 28207
Alliance Urology Specialists, P.A. Greensboro North Carolina 27403
Carolina Urologic Research Myrtle Beach South Carolina 29572
Integrity Medical Research Mountlake Terrace Washington 98043
Wheaton Franciscan Medical Group - Milwaukee Urogynecology Wauwatosa Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01369485, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 10, 2014 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01369485 live on ClinicalTrials.gov.

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