Treatment of Pelvic Organ Prolapse by PIVS Versus Surgeon Cut Mesh
Withdrawn
- Conditions
- Pelvic Floor Prolapse
- Registration Number
- NCT01387685
- Lead Sponsor
- Western Galilee Hospital-Nahariya
- Brief Summary
Women with pelvic floor prolapse who underwent surgery with mesh will be enrolled. The investigators will compare data from the chart, telephone interviews and physical examinations between those who underwent mesh placement to those who underwent placement of PIVS.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
- Women who underwent surgery for pelvic floor prolapse
Exclusion Criteria
- Women who did not have surgery for pelvic floor prolapse.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Satisfaction with study outcome six to twelve months after surgery
- Secondary Outcome Measures
Name Time Method Side effects of the surgery: pain, vaginal erosion by tape, bleeding Within six to twelve months after study
Trial Locations
- Locations (2)
Department of Obstetrics and Gynecology, Western Galilee Hospital
🇮🇱Nahariya, Israel
Dr Neuman clinic
🇮🇱Tel Aviv, Israel