The effectiveness of vaginal prolapse repair employing mesh augmentation.

Completed

• Conditions: Vaginal prolapse; Reproductive Health and Childbirth - Other reproductive health and childbirth disorders

• Registration Number: ACTRN12605000621617
• Lead Sponsor: Johnson and Johnson

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2005-10-10
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 128

Inclusion Criteria

Women with posterior and anterior vaginal wall prolapse with at least one site being of stage 2 or more.(ICS quantitative pelvic organ prolapse examination system).Women with cocomitant urinary symptoms and /or anorectal symptoms maybe included.Women requiring anterior and posterior repair.Women with urodynamic stress incontinence will be offered a mid urethral sling procedure.Willingness to participate.

Exclusion Criteria

Women with apical or vault prolapse of stage 2 or more(ICS quantitative pelvic organ porlapse examination system).Medically unfit for surgery.Women undergoing concomittant abdominal surgery for prolapse eg abdominal sacral colpopexy, Paravaginal repair.Refusal to participate.

Study & Design

• Study Type: Interventional
• Study Design: Not specified