Evaluation of Efficacy and Safety of Urogynecology Synthetic Mesh Surgery in Women With Pelvic Organ Prolapse
Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
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.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 30
Maximum Age: 100
Healthy Volunteers: f
View:
• Pelvic organ prolapse patients with objective / subjective voiding dysfunctions
• Underwent surgery for symptomatic POP ≥ stage II (POP-Q system)
Locations
Other Locations
Taiwan
Department of Obstetrics and Gynecology
RECRUITING
New Taipei City
Contact Information
Primary
Hui-Hsuan Lau, M.D.
huihsuan1220@gmail.com
+886-975-835928
Time Frame
Start Date: 2022-08-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 150
Treatments
mesh surgery
Data obtained before the operation
Robotic-assisted sacrocolpopexy
Data obtained before the operation
a hysterectomy with trans-vaginal mesh repair (Surelift®, Neomedic International, Barcelona, Spain)
Data obtained before the operation
Related Therapeutic Areas
Sponsors
Leads: Mackay Medical College