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Withdrawn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

Study Timeline

• Study Start: 2009-02
• Study First Submitted: 2011-06-29
• Study First Submitted QC: 2011-06-30
• Study First Posted: 2011-07-04
• Primary Completion: 2013-01
• Study Completion: 2013-01
• Status Verified: 2014-06
• Last Update Submitted: 2014-06-19
• Last Update Posted: 2014-06-20

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• Status: WITHDRAWN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