Clinical Trials Directory

Trials / Completed

CompletedNCT05715489

Pectopexy Surgery Without Mesh

Evaluation of the Results of Laparoscopic Pectopexy Surgery Without Using Mesh

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
38 (actual)
Sponsor
Gaziosmanpasa Research and Education Hospital · Other Government
Sex
Female
Age
30 Years – 75 Years
Healthy volunteers
Accepted

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.

Detailed 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).

Conditions

Interventions

TypeNameDescription
PROCEDUREComparison of pre and postoperative POP-Q values of the patientsPectopexy Without Using Mesh will be applied to the patients and POP-Q values will be compared pre and postoperatively
PROCEDUREComparison of pre and postoperative PISQ-12 scores of the patientsPectopexy Without Using Mesh will be applied to the patients and PISQ-12 scores will be compared pre and postoperatively

Timeline

Start date
2022-05-11
Primary completion
2024-05-11
Completion
2024-05-11
First posted
2023-02-08
Last updated
2024-10-01

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05715489. Inclusion in this directory is not an endorsement.