Pectopexy Surgery Without Mesh

Status Recruiting

Clinical Trial Summary

it is aimed to examine the effect of laparoscopic pectopexy surgery without mesh on Pelvic Organ Prolapse Measurement (POP-Q) and quality of life of the patient.

Clinical Trial Description

Every gynecological patient with prolapse is evaluated with POP-Q staging. The POP-Q staging to be performed before the laparoscopic pectopexy operation without mesh (performed by using non-melting sutures with natural tissue repair) performed on the patients will be compared with the POP-Q staging that will be performed 6 months after the operation. In addition, the quality of life of patients before and 6 months after the operation will be compared with the incontinence quality of life scale questionnaire of Pelvic Organ Prolapse / Incontinence Sexual Questionnaire (PISQ-12). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05715489
Study type	Interventional
Source	Gaziosmanpasa Research and Education Hospital
Contact	Suleyman Salman
Phone	+905059345470
Email	sleymansalman@gmail.com
Status	Recruiting
Phase	N/A
Start date	May 11, 2022
Completion date	May 11, 2024

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See also
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