Clin2
NCT04829175Possibly a fitRecruiting

Pelvic mesh follow-up registry for stress leaks and/or prolapse

Stress Urinary IncontinencePelvic Organ Prolapse

Part of Kidney & urinary, Women’s health & pregnancy clinical trials.

This registry follows women having pelvic repair surgery that uses synthetic mesh or a synthetic sling. It helps track outcomes over time and may reassure patients that long-term safety and results are being monitored.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
1,000 people
Ages
21 years and older
Study type
Observational

Who can take part

  • You are a woman age 21 or older
  • You have either stress urinary incontinence (leak with activity) or pelvic organ prolapse symptoms (pelvic dropping/pressure), or both
  • Your planned surgery uses a synthetic (man-made) pubo-urethral sling for leaks and/or synthetic mesh for prolapse
  • This is your planned primary (first) surgery for these problems, not a surgery replacing a prior sling/mesh
  • You can attend required follow-up visits and complete questionnaires
  • You will sign consent to join the follow-up registry

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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