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New registry to track artificial sphincter success in women

NCT ID NCT04114266

First seen Feb 02, 2026 · Last updated May 23, 2026 · Updated 13 times

Summary

This study follows 180 women who receive an artificial urinary sphincter to treat stress incontinence caused by a weak urethra. Researchers will track how many women become dry (using no pads or just one light security pad) and how long that dryness lasts over 5 years. The goal is to better understand the long-term success of this surgical approach.

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Contacts and locations

Locations

  • Addenbrooks Hospital

    Cambridge, United Kingdom

  • CHU Nancy

    Vandœuvre-lès-Nancy, France

  • CHU Rangueil

    Toulouse, France

  • CHU de Lille

    Lille, France

  • CHU de Limoges

    Limoges, France

  • Clinique urologique CHU de NANTES

    Nantes, France

  • Hospital de La Princesa

    Madrid, Spain

  • Hôpital Lyon Sud

    Lyon, France

  • Hôpital de la Pitié-Salpêtrière

    Paris, France

  • Hôpital la Conception

    Marseille, France

  • Klinikum Lippe

    Detmold, Germany

  • Maastricht UMC+

    Maastricht, Netherlands

  • Marqués de Valdecilla University Hospital

    Santander, Spain

  • Thomayer Hospital

    Prague, Czechia

  • Universitair Ziekenhuis Gent

    Ghent, Belgium

  • University Hospital Bordeaux

    Bordeaux, France

  • University Hospital Leuven

    Leuven, 3000, Belgium

  • University Hospital of Nimes

    Nîmes, France

  • University of Rennes, Department of Urology

    Rennes, 35000, France

Conditions

Explore the condition pages connected to this study.