Post-hysterectomy Vaginal Cuff Prolapse Repair

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorKanuni Sultan Suleyman Training and Research Hospital

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 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 criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Laparoscopic Lateral Suspension
  • Laparoscopic Sacrocolpopexy

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Kanuni Sultan Suleyman Training and Research Hospital

Lead sponsor

Başakşehir Çam & Sakura City Hospital

Sponsor institution