Pelvic mesh registry tracks 1,000 women for a decade

NCT ID NCT04829175

First seen Sep 30, 2025 · Last updated May 13, 2026 · Updated 29 times

Summary

This study follows 1,000 women who have had surgery using Ethicon pelvic mesh products for stress urinary incontinence or pelvic organ prolapse. Researchers will check how well the mesh works and how safe it is over 5 to 10 years after surgery. The goal is to better understand long-term outcomes and risks.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Bio-Medical University Rome

    RECRUITING

    Rome, Italy

  • Duke University

    RECRUITING

    Durham, North Carolina, 27707, United States

  • Herlev Hospital

    NOT_YET_RECRUITING

    Hillerød, Denmark

  • Hopital Jeanne de Flandres

    NOT_YET_RECRUITING

    Lille, France

  • Karolinska Institute

    RECRUITING

    Stockholm, Sweden

  • Krankenhaus der barmherzigen Schwestern

    RECRUITING

    Linz, Austria

  • UPMC

    RECRUITING

    Pittsburgh, Pennsylvania, 15213, United States

  • Universitatsklinikum Tubingen

    RECRUITING

    Tübingen, Germany

  • University of Pennsylvania

    RECRUITING

    Philadelphia, Pennsylvania, 19104, United States

  • Yale University

    RECRUITING

    New Haven, Connecticut, 06510, United States

Conditions

Explore the condition pages connected to this study.