Clinical Trial

Laparoscopic Pectopexy and Laparoscopic Colporrhaphies in Pelvic Organ Prolapse Treatment

Enrolling by Invitation
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Summary
This prospective cohort study investigates the surgical outcomes of laparoscopic pectopexy and laparoscopic colporraphy performed at the Wellbeing Services County of South Ostrobothnia. The primary outcome measure is to assess changes in sensation of bulge and pressure. Secondary outcome measures include evaluating other prolapse symptoms and pain, quality of life, anatomical correction of prolapse, surgical safety parameters, and postoperative complications. Approximately 40-50 laparoscopic pectopexies will be performed over two years by a single experienced surgeon. The study requires preoperative and postoperative assessments, including standardized patient questionnaires and anatomical measurements.
Trial Details
NCT Number NCT06902909
Lead Sponsor Tampere University Hospital
Collaborators: Seinajoki Central Hospital
Conditions Vaginal Vault Prolapse, Uterine Prolapse, Cystocele, Midline, Rectocele; Female
Enrollment 50 participants
Start Date 2024-02-01
Primary Completion 2027-02-28 (estimated)
Study Completion 2027-02-28 (estimated)
Updated on ClinicalTrials.gov 2025-03-30