Laparoscopic procedure for treating female stress incontinence
Evaluation of the Results of Laparoscopic Extraperitoneal ( Modified) Burch
This study tests a new laparoscopic surgery to see if it helps women with stress urinary incontinence feel better and improve their quality of life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 25 Years to 75 Years |
| Sex | Female |
| Sponsor | Gaziosmanpasa Research and Education Hospital Government |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT05768607 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of a modified laparoscopic extraperitoneal Burch colposuspension technique for women suffering from stress urinary incontinence. The study compares pre- and postoperative urodynamics, surgical outcomes, and complications in patients undergoing this procedure at Istanbul Health Sciences University Gaziosmanpasa Training and Research Hospital. Additionally, it assesses the quality of life and impact of urinary incontinence using validated questionnaires before and six months after surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are women diagnosed with stress urinary incontinence.
Not a fit: Patients with a history of urogynecological surgery or significant pelvic pathology may not benefit from this study.
Why it matters
Potential benefit: If successful, this procedure could provide a less invasive and more efficient treatment option for women with stress urinary incontinence.
How similar studies have performed: Other studies have shown success with laparoscopic techniques for stress incontinence, but the modified approach being tested may offer novel benefits.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * having stress urinary incontinence Exclusion Criteria: * having any kind of urogynecological surgery history * having pelvic mass * having endometrial or myometrial pathology * having uterine prolapsus grater than grade 2 * benign obese
Where this trial is running
Istanbul
- Gaziosmanpasa Training and Research Hospital — Istanbul, Turkey (Recruiting)
Study contacts
- Study coordinator: Suleyman Salman
- 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.