Prolift Versus IVS for Pelvic Floor Prolapse

Western Galilee Hospital-Nahariya

Status: Withdrawn

Conditions: Pelvic Floor Prolapse

Study type: Observational

Funder types: Other

Identifiers

NCT01383291

920090041

Details and patient eligibility

About

• 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.

Sex: Female

Ages: 18 to 95 years old

Volunteers: No Healthy Volunteers

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

Trial design

0 participants in 1 patient group

Pelvic floor prolapse

Description:

Those who underwent prolift and those who underwent IVS