Prolift Versus IVS for Pelvic Floor Prolapse
Withdrawn
- Conditions
- Pelvic Floor Prolapse
- Registration Number
- NCT01383291
- Lead Sponsor
- Western Galilee Hospital-Nahariya
- Brief Summary
* Women who underwent mesh or sling procedures to correct pelvic organ prolapse will be enrolled.
* Their data will be collected from the files.
* Comparison between two groups will be carried our: Those who underwent a posterior IVS and those who underwent posterior prolift procedure.
* The data will be obtained by questionaires by a telephone interview by a physician who did not participate in the surgery.
* Follow-up physical examination data will also be obtained.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
- Women who previously underwent surgery for pelvic floor prolapse at least a year before
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
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
Clinics of Dr Neuman
🇮🇱Rishon Lezion, Israel
Department of Obstetrics and Gynecology, Western Galilee Hospital
🇮🇱Nahariya, Israel