Laparoscopic Lateral Suspension Versus Laparoscopic Sacrocolpopexy for Post-Hysterectomy Vaginal Cuff Prolapse: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
Turkey
Basaksehir Cam and Sakura City Hospital
RECRUITING
Istanbul
Contact Information
Primary
Ozan Karadeniz, MD
dr.ozankrdnz@gmail.com
+905333663003
Time Frame
Start Date: 2025-09-30
Estimated Completion Date: 2026-10-15
Participants
Target number of participants: 50
Treatments
Active_comparator: Laparoscopic Sacrocolpopexy
Experimental: Laparoscopic Lateral Suspension
Sponsors
Leads: Kanuni Sultan Suleyman Training and Research Hospital

This content was sourced from clinicaltrials.gov