Actively Recruiting
Post-Hysterectomy Vaginal Length: Horizontal vs. Vertical Closure
Led by Gaziosmanpasa Research and Education Hospital · Updated on 2025-07-16
62
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This prospective clinical study aims to evaluate the impact of vaginal cuff closure orientation-horizontal versus vertical-on postoperative total vaginal length in patients undergoing vaginal hysterectomy combined with lateral suspension. By comparing anatomical outcomes between the two closure techniques, the study seeks to determine which method better preserves vaginal length, potentially influencing surgical preferences and postoperative quality of life.
CONDITIONS
Official Title
Post-Hysterectomy Vaginal Length: Horizontal vs. Vertical Closure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women undergoing vaginal hysterectomy and lateral suspension surgery for stage 3-4 uterine prolapse
- Agree to participate and sign the informed consent form
You will not qualify if you...
- Previous suspension surgeries for uterine prolapse such as sacrospinous ligament fixation, sacrocolpopexy, or high sacrouterine plication
- Vaginal hysterectomy performed due to malignancy
- History of radiotherapy for malignancy (brachytherapy)
- Severe vaginal atrophy making surgery unsuitable
- Unable to comply with follow-up visits
- Decline to participate or do not sign the informed consent form
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Gaziosmanpaşa Training and Research Hospital
Istanbul, Turkey (Türkiye)
Actively Recruiting
Research Team
S
serkan kumbasar, md
CONTACT
E
ecenur çelikoğlu, md
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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