Clinical Trial

VNOTES Approach in Mesh Free Sacrocolpopexy: A Functional and Anatomic Evaluation

Study acronym: vnotes
Recruiting
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Record status
This record was last updated August 11, 2025 (before its estimated January 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
This study aims to evaluate the effectiveness of mesh-free sacrocolpopexy performed using the VNOTES (Vaginal Natural Orifice Transluminal Endoscopic Surgery) technique in the surgical treatment of pelvic organ prolapse. Anatomical and functional outcomes will be assessed over a 6-month period before and after the operation. Evaluation tools will include the Pelvic Floor Distress Inventory-20 (PFDI-20), Pelvic Organ Prolapse Quantification (POP-Q) system, and the Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12). The findings of this study are expected to provide important data on the anatomical improvement, functional outcomes, and impact on sexual function of mesh-free sacrocolpopexy performed via the VNOTES approach.
Trial Details
NCT Number NCT07114029
Lead Sponsor Gaziosmanpasa Research and Education Hospital
Conditions Pelvic Organ Prolapse
Enrollment 26 participants
Start Date 2025-07-01
Primary Completion 2026-01-01 (estimated)
Study Completion 2026-01-01 (estimated)
Updated on ClinicalTrials.gov 2025-08-11