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

Not Applicable

Recruiting

• Conditions: Pelvic Organ Prolapse
• Interventions: Procedure: Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh

• Registration Number: NCT06176521
• Lead Sponsor: Gaziosmanpasa Research and Education Hospital

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

Detailed Description

Not available

Study Timeline

• Study Start: 2023-11-01
• Study First Submitted: 2023-12-09
• Study First Submitted QC: 2023-12-09
• Study First Posted: 2023-12-19
• Status Verified: 2024-11
• Primary Completion: 2024-12-01
• Last Update Submitted: 2025-01-04
• Last Update Posted: 2025-01-07
• Study Completion: 2025-11-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: Female
• Target Recruitment: 35

Inclusion Criteria

1. being 18 years old or older
2. needing an operation for symptomatic pelvic organ prolapse -

Exclusion Criteria

1. past history of chemotherapy or radiotherapy
2. past history of pelvic organ prolapse surgery
3. if there is a contraindication of laparoscopy -

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh	Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh	-

Primary Outcome Measures

Name	Time	Method
Pre and post operative assessment of POP-Q measurements	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	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.

Trial Locations

Locations (1)

Gaziosmanpasa Training and Research Hospital; 🇹🇷 Istanbul, Turkey