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Clinical trialNCT03556891CompletedInterventional

Pivotal Study of eCoin for Overactive Bladder With Urgency Urinary Incontinence

SponsorValencia Technologies CorporationEnrollment133Incontinence, UrinaryOveractive BladderUrge IncontinenceUrinary Urge Incontinence
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

15 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Kaiser Permanente

    Downey, California, United States

  • Sequoia Urology Center

    Redwood City, California, United States

  • Kaiser Permanente

    San Diego, California, United States

  • Sansum Clinic

    Santa Barbara, California, United States

  • Surgone Pc

    Englewood, Colorado, United States

  • Urology Associates of Norwalk

    Norwalk, Connecticut, United States

  • Florida Bladder Institute

    Naples, Florida, United States

  • North Shore Medical Group

    Skokie, Illinois, United States

  • Unitypoint Clinic

    Waterloo, Iowa, United States

  • Chesapeake Urology

    Owings Mills, Maryland, United States

  • Adult & Pediatric Urology

    Omaha, Nebraska, United States

  • Manhattan Medical Research

    New York, New York, United States

  • Alliance Urology Specialists

    Greensboro, North Carolina, United States

  • the Institute for Female Pelvic Medicine & Reconstructive Surgery (fpm Institute)

    Allentown, Pennsylvania, United States

  • South Carolina Ob/gyn

    Columbia, South Carolina, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
4 Sept 2018
Primary completion
12 Apr 2020
Completion
18 Sept 2024
Last update posted
2 Oct 2025
Registered enrollment
133
Registry id
NCT03556891

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.