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Completed Not applicable Interventional Results available

Pivotal Study of eCoin for Overactive Bladder With Urgency Urinary Incontinence

ClinicalTrials.gov ID: NCT03556891

Public ClinicalTrials.gov record NCT03556891. 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 Oct 29, 2026, 6:28 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

Pivotal Study of Subcutaneous Tibial Nerve Stimulation With eCoin for Overactive Bladder (OAB) With Urgency Urinary Incontinence (UUI)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial is a prospective, multicenter, single-arm study of the safety and effectiveness of eCoinTM tibial nerve stimulation in subjects having overactive bladder (OAB) with urgency urinary incontinence (UUI). The study will evaluate changes from baseline in OAB symptoms as measured by voiding diaries and patient reported-outcomes through 48 weeks of eCoinTM therapy or 52 weeks of implantation.

Study identification

NCT ID
NCT03556891
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
133 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Sep 4, 2018 (Actual)
Primary completion
Apr 12, 2020 (Actual)
Completion
Sep 18, 2024 (Actual)
Last update posted
Oct 2, 2025

2018 – 2024

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Kaiser Permanente Downey California 90242 —
Sequoia Urology Center Redwood City California 94062 —
Kaiser Permanente San Diego California 92110 —
Sansum Clinic Santa Barbara California 93105 —
SurgOne PC Englewood Colorado 80113 —
Urology Associates of Norwalk Norwalk Connecticut 06850 —
Florida Bladder Institute Naples Florida 34109 —
North Shore Medical Group Skokie Illinois 60076 —
UnityPoint Clinic Waterloo Iowa 50703 —
Chesapeake Urology Owings Mills Maryland 21117 —
Adult & Pediatric Urology Omaha Nebraska 68114 —
Manhattan Medical Research New York New York 10016 —
Alliance Urology Specialists Greensboro North Carolina 27403 —
The Institute for Female Pelvic Medicine & Reconstructive Surgery (FPM Institute) Allentown Pennsylvania 18103 —
South Carolina OB/GYN Columbia South Carolina 29201 —

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 NCT03556891, 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 Oct 2, 2025 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03556891 live on ClinicalTrials.gov.

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