Comparison of Laparoscopic Pectopexy and Laparoscopic Lateral Suspension Surgeries

Sponsor
Gaziosmanpasa Research and Education Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05930795
Collaborator
(none)
80
1
2
13
6.1

Study Details

Study Description

Brief Summary

There is not a study in the literature comparing laparoscopic pectopexy and laparoscopic lateral suspension (LLS) surgeries in the surgical treatment of pelvic organ prolapse. However, there are studies comparing the efficacy of other surgery types for pelvic organ prolapse. For example,In a study, the clinical and anatomical success rate in LLS operations was 83.8%, while the success rate in abdominal sacropexy operation was 89.2%.In another study in which pectopexy and vaginal sacro spinous fixation operations were compared, apical prolapse recurrence rates were found to be similar in both groups.

Condition or Disease Intervention/Treatment Phase
  • Procedure: pectopexy
  • Procedure: lateral suspension
N/A

Detailed Description

Pelvic organ prolapse (POP) can be defined as the protrusion of the pelvic organs out of the vagina. Many women experience the symptoms of prolapse of the pelvic organs during their daily activities, during sexual intercourse or during exercise. POP causes various undesirable effects in terms of sexual life and body aesthetics in women. With the increase in the number of elderly individuals in societies, the prevalence of prolapse cases is increasing and is becoming more common.

Patients who had laparoscopic pectopexy operation due to minimum POPQ stage 2 according to the International Classification of Pelvic Organ Prolapse Quantification (POP Q) in our hospital and who had ls lateral suspension surgery with the same indication were planned to be included retrospectively. In the first group, patients who had laparoscopic pectopexy operation were planned to be included. In the second group, it was planned to include patients who had ls lateral suspension operation.

Demographic and intra operative data collected before the procedure: (operation time, estimated blood loss, hospital stay, bowel and bladder injury) and intra operative and postoperative complications and recurrence rates and anatomically preoperative and post op Pelvic prolapse (with POP-Q classification), PopQ values (minimum 6 months) were aimed to be compared between two groups to assess anatomic comparement. Furthermore, the patients will be called back and Pelvic Organ Prolapse / Incontinence Sexual Questionnaire (PİS-Q) questionnaire will be applied to both groups and the results will be compared prospectively to assess functional results.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Screening
Official Title:
Evaluation of the Comparison of Anatomical and Functional Results of Laparoscopic Pectopexy and Laparoscopic Lateral Suspension Surgeries for the Treatment of Pelvic Organ Prolapse
Actual Study Start Date :
Aug 10, 2022
Anticipated Primary Completion Date :
Aug 10, 2023
Anticipated Study Completion Date :
Sep 10, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Patients with pelvic organ prolapse undergone pectopexy surgery

Procedure: pectopexy
pectopexy: surgery performed by suspending prolapsed uterus or vault to the pectineal ligament
Other Names:
  • surgery performed by suspending prolapsed uterus or vault to the pectineal ligament
  • Active Comparator: Patients with pelvic organ prolapse undergone lateral suspension surgery

    Procedure: lateral suspension
    lateral suspension: surgery performed by suspending prolapsed uterus or vault to the lateral walls of the abdomen corresponding to the 3 cm anterior superior to the iliac crest

    Outcome Measures

    Primary Outcome Measures

    1. Comparison of pre and post operative assessment of POP-Q measurements [1 year]

      Comparison of POP-Q values of patients undergone pectopexy and lateral suspension pre and postoperatively.

    2. Comparison of Pre and post operative assessment of Pelvic Organ Prolapse / Incontinence Sexual Questionnaire [1 year]

      Units on a scale of the patients obtained with Pelvic Organ Prolapse / Incontinence Sexual Questionnaire will be compared before and after surgery. PISQ- 12 is a Likert type of survey with five options (scoring from 0 to 4) in each question and the patient is asked a total of 12 questions. The total score is calculated by summing points given to each question. A higher score means better sexual function and the highest total score is 48.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patients with POP Q stage 2 and above, operated for symptomatic pelvic organ prolapse,

    • Being a Citizen of the Republic of Turkey over the age of 18

    • Patients operated by the same experienced surgeons

    Exclusion Criteria:
    • To have received chemotherapy and/or radiotherapy for any reason before

    • Having previously operated for prolapse

    • Cases with Contraindications for Laparoscopy

    • Cases with severe cardiovascular or respiratory disease

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Gaziosmanpasa Training and Research Hospital Istanbul Turkey

    Sponsors and Collaborators

    • Gaziosmanpasa Research and Education Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Serkan Kumbasar, Principal Investigator, Gaziosmanpasa Research and Education Hospital
    ClinicalTrials.gov Identifier:
    NCT05930795
    Other Study ID Numbers:
    • GaziosmanpaşaTREHv
    First Posted:
    Jul 5, 2023
    Last Update Posted:
    Jul 5, 2023
    Last Verified:
    Jun 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 5, 2023