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Efficacy/Safety of Urogynecology Synthetic Mesh Surgery

Recruitingn/aAges 30 Years - 100 YearsFemaleMackay Medical College
NCT05682989 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This is a retrospective cohort study, aiming at analyzing the efficacy and safety of mesh surgery in pelvic organ prolapse. The synthetic mesh for pelvic organ prolapse include transvaginal mesh or laparotomy, laparoscope, or robotic-assisted laparoscopic sacrocolpopexy with mesh augmentation. The investigators would like to evaluate the efficacy and safety, such as recurrence rates and complication rates for women who underwent urogynecology mesh surgery.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Pelvic organ prolapse patients with objective / subjective voiding dysfunctions * Underwent surgery for symptomatic POP ≥ stage II (POP-Q system) Exclusion Criteria: * Patients with a history of pelvic radiation. * Patients with a history of vesico-/recto-/urethra-vaginal fistula * Patients unable to be followed up.
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What it tests

  • Urodynamic investigations before and after a mesh surgery protocol.
  • Urodynamic investigations before and after a robotic-assisted sacrocolpopexy protocol.
  • Urodynamic investigations before and after a hysterectomy with trans-vaginal mesh repair
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Where

1 site
Department of Obstetrics and Gynecology
New Taipei City, Taiwan
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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