Evaluation of the Results of Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh in the Surgical Treatment of Pelvic Organ Prolapse

Gaziosmanpasa Research and Education Hospital1 site in 1 country35 target enrollmentNovember 1, 2023

ConditionsPelvic Organ Prolapse

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Pelvic Organ Prolapse
Sponsor: Gaziosmanpasa Research and Education Hospital
Enrollment: 35
Locations: 1
Primary Endpoint: Pre and post operative assessment of POP-Q measurements
Status: Completed
Last Updated: 8 months ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

Evaluation of the anatomical and functional results of laparoscopic sacrohysteropexy and sacrocolpopexy surgeries performed without using mesh in the surgical treatment of pelvic organ prolapse

Registry

clinicaltrials.gov

Start Date

November 1, 2023

End Date

June 1, 2025

Last Updated

8 months ago

Study Type

Interventional

Study Design

Single Group

Sex

Female

Investigators

Sponsor

Gaziosmanpasa Research and Education Hospital

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•being 18 years old or older
•needing an operation for symptomatic pelvic organ prolapse -

Exclusion Criteria

•past history of chemotherapy or radiotherapy
•past history of pelvic organ prolapse surgery
•if there is a contraindication of laparoscopy -

Outcomes

Primary Outcomes

Pre and post operative assessment of POP-Q measurements

Time Frame: 1 year

POP-Q values of patients before and after laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh on Pelvic Organ Prolapse will be compared.

Pre and post operative assessment of Pelvic Organ Prolapse / Incontinence Sexual

Time Frame: 1 year

Units on a scale of the patients obtained with Pelvic Organ Prolapse / Incontinence Sexual Questionnaire (PISQ-12) will be compared before and after surgery.