Pelvic mesh registry aims to track outcomes over a decade

NCT ID NCT04829175

First seen Jun 27, 2026 · Last updated Jul 07, 2026 · Updated 2 times

Summary

This study is a long-term registry that will follow 1,000 women who receive pelvic mesh products for stress urinary incontinence or pelvic organ prolapse. Researchers will track how well the mesh works and any complications over 5 to 10 years. The goal is to gather real-world data on safety and effectiveness.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to
If successful, this registry could provide reliable long-term safety and effectiveness data for pelvic mesh products, helping doctors and patients make informed decisions.
What could go wrong
This is an observational registry, not a controlled trial, so it cannot prove cause and effect. Results may take years and could show complications or limited benefit.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

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

    ACTIVE_NOT_RECRUITING

    Tübingen, Germany

  • University of Pennsylvania

    RECRUITING

    Philadelphia, Pennsylvania, 19104, United States

  • Yale University

    RECRUITING

    New Haven, Connecticut, 06510, United States

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