Clinical Trial

Efficacy/Safety of Urogynecology Synthetic Mesh Surgery

Recruiting

Record status

This record was last updated April 5, 2023 (before its estimated August 1, 2023 completion). Its status may not reflect the trial's current state.

Summary

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.

Protocol Amendment History 2 amendments

This ClinicalTrials.gov record has been amended 2 times since 2023-01-11; most recent amendment 2023-04-02.

Trial Details

NCT Number	NCT05682989
Lead Sponsor	Mackay Medical College
Conditions	Pelvic Organ Prolapse, Stage III and IV High Grade Pelvic Organ Prolapse
Enrollment	150 participants
Start Date	2022-08-01
Primary Completion	2023-08-01 (estimated)
Study Completion	2027-12-31 (estimated)
Updated on ClinicalTrials.gov	2023-04-05