← Eichor
Study identifier: NCT07174921 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Post-hysterectomy Vaginal Cuff Prolapse Repair

Condition: Vaginal Cuff Complications  ·  Sponsor: Kanuni Sultan Suleyman Training and Research Hospital

PhaseNA
Planned participants50
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is a randomized controlled trial comparing two minimally invasive surgeries-laparoscopic lateral suspension and laparoscopic sacrocolporopexy-for women who develop vaginal cuff prolapse after hysterectomy. Vaginal cuff prolapse occurs when the top of the vagina loses support after the uterus is removed, which can cause discomfort, bulging, or urinary and bowel problems. The goal of this study is to determine which surgical approach is safer, more effective, and improves quality of life for patients. Women enrolled in the trial will be randomly assigned to one of the two surgeries, and outcomes such as prolapse recurrence, complications, recovery time, and patient satisfaction will be carefully monitored. By comparing these two techniques, this study aims to provide clear guidance for surgeons and patients to make informed decisions about the best surgical treatment for post-hysterectomy vaginal cuff prolapse.

This description comes directly from the study's public registry record.

Talk to the study team

Ozan Karadeniz, MD  ·  +905333663003  ·  dr.ozankrdnz@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Basaksehir Cam and Sakura City HospitalIstanbul, Istanbul, Turkey (Türkiye)Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07174921