Actively Recruiting
VNOTES Approach in Mesh Free Sacrocolpopexy: A Functional and Anatomic Evaluation
Led by Gaziosmanpasa Research and Education Hospital · Updated on 2025-08-11
26
Participants Needed
2
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
VNOTES Approach in Mesh Free Sacrocolpopexy: A Functional and Anatomic Evaluation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 18 to 75 years
- Diagnosed with apical and anterior pelvic organ prolapse stage 2 or higher
- Have symptoms of pelvic organ prolapse and are candidates for surgery
- Undergoing surgery performed by experienced surgeons
- Citizens of the Republic of Turkey
You will not qualify if you...
- Previous chemotherapy and/or radiotherapy for any cancer
- Previous surgery for pelvic organ prolapse
- Severe cardiovascular or respiratory diseases
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Gaziosmanpaşa Training and Research Hospital
Istanbul, Turkey (Türkiye)
Actively Recruiting
2
Gaziosmanpaşa Training and Research Hospital
Istanbul, Turkey (Türkiye)
Actively Recruiting
Research Team
Y
yağmur acıyiyen, md
CONTACT
E
ecenur çelikoğlu, md
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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