Evaluation of Anatomical Results and Sexual Functions After Unilateral and Bilateral Laparoscopic Suture Sacro-hysteropexy Operations

Phase

N/A

Condition

Genitourinary Prolapse

Treatment

bilateral suture sacro-hysteropexy

unilateral suture sacro-hysteropexy

Clinical Study ID

NCT06341088

B.30.2.ATA.0.01.00/132

Ages 18-60
Female
Accepts Healthy Volunteers

Study Summary

The study was planned as prospective and randomized. For the study, patients will be randomized into two groups as unilateral and bilateral suture sacro-hysteropexy operations.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Patients between the ages of 18-60
No previous prolapse surgery
Not having a chronic disease
Having stage 3-4 prolapse

Exclusion

Exclusion Criteria:

Outside the age range of 18-60 years
Previous prolapse surgery
Having early stage (1-2) prolapse
History of chronic disease

Study Design

bilateral suture sacro-hysteropexy

April 05, 2024

February 05, 2025

Study Description

The study was planned as prospective and randomized. For the study, patients will be randomized into two groups as unilateral and bilateral suture sacro-hysteropexy operations.Computerized random number table will be used as randomization method. Patients who agree to participate in the study and fulfill the inclusion criteria will be evaluated on the effects of prolapse on quality of life and sexual function before and after the surgical procedures and their complaints and satisfaction will be questioned. Surgical success and complications will be evaluated. Changes in the level of prolapse will be evaluated.

Connect with a study center

Atatürk University
Erzurum, Palandöken
Turkey
Site Not Available

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