Pectopexy Surgery Without Mesh

Evaluation of the Results of Laparoscopic Pectopexy Surgery Without Using Mesh

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05715489

Enrollment

Registered

2023-02-08

Start date

2022-05-11

Completion date

2024-05-11

Last updated

2024-10-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Organ Prolapse

Brief 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).

Interventions

PROCEDUREComparison of pre and postoperative POP-Q values of the patients

Pectopexy 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 patients

Pectopexy Without Using Mesh will be applied to the patients and PISQ-12 scores will be compared pre and postoperatively

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

30 Years to 75 Years

Healthy volunteers

Yes

Inclusion criteria

* having pelvic organ prolapse greater than stage 2 according to POP-Q evaluation system * being sexually active

Exclusion criteria

* Disease requiring chronic steroid use * Asthma * Having chronic obstructive pulmonary disease * Having malignancy, * Having metabolic and rheumatological diseases that impair tissue healing, such as scleroderma

Design outcomes

Primary

Measure	Time frame	Description
Pre and post operative assessment of POP-Q measurements	2 year	POP-Q values of patients before and after laparoscopic pectopexy surgery without mesh on Pelvic Organ Prolapse will be compared.
Pre and post operative assessment of Pelvic Organ Prolapse / Incontinence Sexual	2 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026