findmyKOL
Clinical trialNCT05250908Active, not recruitingInterventional

INTIBIA Pivotal Study

SponsorColoplast A/SEnrollment208Lower Urinary Tract SymptomsUrinary Bladder DiseasesUrinary Bladder, OveractiveUrinary Incontinence, UrgeUrologic DiseasesUrological Manifestations
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Prospective, randomized, double-blind, multicenter study to evaluate the safety and efficacy of an implantable tibial nerve stimulator in subjects with urgency urinary incontinence (UUI).

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

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

Netherlands
  • Bergman Clinics, Women'S Health, Department of Gynecology

    Amsterdam, Netherlands

  • Isala Zwolle

    Zwolle, Netherlands

United States
  • Cedars-Sinai Medical Group

    Beverly Hills, California, United States

  • Urology Group of Southern California

    Los Angeles, California, United States

  • Medstar Washington Hospital Center

    Washington D.C., District of Columbia, United States

  • Advanced Urology Associates

    Daytona Beach, Florida, United States

  • Southeastern Urogynecology & Pelvic Surgery

    Moultrie, Georgia, United States

  • Rosemark Womencare Specialists

    Idaho Falls, Idaho, United States

  • Cypress Medical Research Center, Llc

    Wichita, Kansas, United States

  • Baystate Medical Center

    Springfield, Massachusetts, United States

  • University of Michigan

    Ann Arbor, Michigan, United States

  • Advanced Urogynecology of Michigan

    Dearborn, Michigan, United States

  • Specialty Clinical Research of St. Louis

    St Louis, Missouri, United States

  • Atlantic Health System - Amg Urology (garden State Urology)

    Denville, New Jersey, United States

  • Wake Forest University

    Winston-Salem, North Carolina, United States

  • the Urology Group

    Cincinnati, Ohio, United States

  • Metrohealth System

    Cleveland, Ohio, United States

  • the Institute for Female Pelvic Medicine and Reconstructive Surgery- Axia Womens Health

    Allentown, Pennsylvania, United States

  • Midlantic Urology

    Bala-Cynwyd, Pennsylvania, United States

  • the Female Pelvic Health Center

    Newtown, Pennsylvania, United States

  • Thomas Jefferson University

    Philadelphia, Pennsylvania, United States

  • Houston Metro Urology

    Houston, Texas, 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
7 Mar 2022
Primary completion
12 May 2025
Completion
27 Jun 2026
Last update posted
2 Mar 2026
Registered enrollment
208
Registry id
NCT05250908

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.