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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age40-80
SponsorKocaeli University

About this trial

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.

Eligibility criteria

Qualifiers

Female patients older than 40 years and younger than 80 years old with symptomatic uterine prolapse

Patients who provided written consent for the surgical procedure

Patients who do not wish to preserve their uterus

Disqualifiers

Patients who cannot obtain anesthesia approval for laparoscopic surgery

Patients who have a confirmed or suspected pregnancy

Patients who have abnormal uterine/cervical/vaginal bleeding

Patients with biopsy-confirmed endometrial hyperplasia or cervical dysplasia

Trial design

Treatments tested in this trial

  • Meshless Laparoscopic Pectopexy
  • Laparoscopic Pectopexy with mesh

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators