Post-hysterectomy Vaginal Cuff Prolapse Repair

Recruiting N/A Interventional Study
Vaginal Cuff Complications
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
50 (estimated)
Sponsor
Kanuni Sultan Suleyman Training and Research Hospital · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
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 thi…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: Women aged ≥18 years. History of hysterectomy (any approach: abdominal, vaginal, or laparoscopic). Symptomatic vaginal cuff prolapse (POP-Q stage ≥ II). Able to provide written informed consent. Willing and able to comply with study procedures and follow-up visits. Exclusio…
Contacts

Ozan Karadeniz, MD

+905333663003

dr.ozankrdnz@gmail.com

CONTACT