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Study identifier: NCT05682989 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Efficacy/Safety of Urogynecology Synthetic Mesh Surgery

Condition: Pelvic Organ Prolapse · Stage III and IV High Grade Pelvic Organ Prolapse  ·  Sponsor: Mackay Medical College

PhaseN/A
Planned participants150
Who can joinFemale, 30 Years to 100 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Hui-Hsuan Lau, M.D.  ·  +886-975-835928  ·  huihsuan1220@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Obstetrics and GynecologyNew Taipei City, TaiwanRecruiting

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Source record: clinicaltrials.gov/study/NCT05682989