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Laparoscopic Pectopexy With and Without Mesh Use for Pelvic Organ Prolapse.

NCT07306715 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2026-02-02

No results posted yet for this study

Summary

Genital apical prolapse refers to the descent of the vaginal apex, uterus, or cervix, and surgical treatment is required for adequate apical support. Laparoscopic pectopexy is a surgical method developed as an alternative to the gold standard, sacrocolpopexy, in the treatment of genital organ prolapse, especially for obese patients for whom dissection is difficult. The vaginal cuff is attached to the pectineal ligament with polypropylene mesh in the standard technique. The use of mesh is subject to serious restrictions due to complications such as mesh erosion. Surgical methods without using a mesh may be safer treatment options for patients with genital prolapse. This study aimed to compare the results of Laparoscopic Pectopexy surgery with and without the use of mesh material after hysterectomy.

Conditions

  • Genital Prolapse

Interventions

PROCEDURE

Meshless Laparoscopic Pectopexy

The vaginal cuff will be fixed to the pectineal ligament with No. 1, non-absorbable Prolene suture.

PROCEDURE

Laparoscopic Pectopexy with mesh

The vaginal cuff will be fixed to the pectineal ligament with polypropylene mesh.

Sponsors & Collaborators

  • Kocaeli University

    lead OTHER

Principal Investigators

  • İsmail Bıyık, M.D. · Kütahya Sağlık Bilimleri University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-29
Primary Completion
2027-04-01
Completion
2027-06-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07306715 on ClinicalTrials.gov