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Clinical Trials in Egypt / NCT07596498
Recruiting Not applicable

Comparison of the Effectiveness and Learning Curve of Laparoscopic Pectopexy Versus Laparoscopic Sacrocolpopexy

NCT07596498 · tracked via the Priya Life Science Egypt tracker
Sponsor
Ain Shams University
Phase
Not applicable
Started
2026-04-01
Last updated
2026-05-19

Condition(s) studied

Apical Prolapse

Investigational drug(s) / intervention(s)

Laparoscopic PectopexyLaparoscopic Sacrocolpopexy

Laparoscopic Pectopexy: to evaluate the effectiveness and learning curve of laparoscopic pectopexy in comparison with laparoscopic sacrocolpopexy for the treatment of apical prolapse performed by the same surgeon.

Laparoscopic Sacrocolpopexy: Laparoscopic Sacrocolpopexy

Study summary

Pelvic organ prolapse, particularly apical prolapse, is a common condition among aging women, and laparoscopic sacrocolpopexy is considered the standard surgical treatment due to its high anatomical success. However, it poses technical challenges and risks related to sacral dissection.

Laparoscopic pectopexy, a newer technique using the iliopectineal ligament for mesh fixation, offers a safer anatomical route with shorter operative time and fewer complications. The previous studies evaluate the sacrocolpopexy and pectopexy are all retrospective. This study is prospective randomized controlled study that adds Comparison on the success rate and learning curve of pectopexy versus sacrocolpopexy .

Eligibility

Sex
FEMALE
Min age
40 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Patients diagnosed with uterine prolapse with POP-Q stage ≥ III. * Patients diagnosed with vault vaginal prolapse with POP-Q stage ≥ III. Exclusion Criteria: * Patients who refuse to participate in the study. * Patients who have isolated anterior or posterior vaginal wall prolapse. * Women who are pregnant or lactating. * Patients with severe comorbidities, including: Serious heart, liver, kidney, or blood diseases or any condition preventing them from tolerating surgery. * Women with a desire to conceive.

Primary outcome measure(s)

  • Pain Assessment — 24 Hours
    To assess the Pain intensity after the operation and the pain will be evaluated using the Visual Analog Scale (VAS) whereas : 0 is no pain, and 10 is worst pain.
  • Number of participants treated — 6 Months
    Treatment of the female patients whom suffering from Apical Prolapse using laparoscopic pectopexy and laparoscopic sacrocolpopexy

Trial sites (1)

FacilityCityRegionStatus
Ain Shams University Hospital Cairo Abbasia Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07596498 on ClinicalTrials.gov ↗ ← All trials in Egypt