Comparing two surgical methods for treating genital prolapse
Comparison of the Effects of Sacrospinous Fixation and V-notes Lateral Suspension Operations on Anatomical Recovery, Effectiveness and Quality of Life.
This study is testing two different surgical methods for treating genital prolapse to see which one helps patients recover better and improves their quality of life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 70 (estimated) |
| Ages | 35 Years to 75 Years |
| Sex | Female |
| Sponsor | Gaziosmanpasa Research and Education Hospital Government |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06307873 on ClinicalTrials.gov |
What this trial studies
This study compares the effects of two surgical techniques, sacrospinous fixation and V-notes lateral suspension, on patients with genital prolapse. It aims to evaluate anatomical recovery, effectiveness, and quality of life outcomes following these procedures. The study will assess pre and post-operative results using the POP-Q and PISQ-12 measures to determine which method yields better results. Conducted at a gynecology and obstetrics clinic, this research seeks to provide insights into optimal surgical approaches for this condition.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 35-75 who do not have pelvic masses or cervical/endometrial lesions.
Not a fit: Patients with pelvic masses, cervical or endometrial lesions, or diagnosed endometrial cancer may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could help identify the more effective surgical option for improving recovery and quality of life in patients with genital prolapse.
How similar studies have performed: While there have been studies on surgical methods for genital prolapse, this specific comparison of sacrospinous fixation and V-notes lateral suspension is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * patient aged 35-75 patients without pelvic mess, servical or endometrial lesion Exclusion Criteria: * patients with pelvic mess, servical or endometrial lesion patient with diagnosed endometrial cancer
Where this trial is running
Istanbul
- Gaziosmanpasa Training and Research Hospital — Istanbul, Turkey (Recruiting)
Study contacts
- Study coordinator: Süleyman Salman, Professor
- Email: sleymansalman@gmail.com
- Phone: +905059345470
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.